116 HR 5279 IH: Cosmetic Safety Enhancement Act of 2019
U.S. House of Representatives
2019-12-03
text/xml
EN
Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.
1.Short title; table of contents
(a)This Act may be cited as the Cosmetic Safety Enhancement Act of 2019
. (b)The table of contents for this Act is as follows:
Sec. 1. Short title; table of contents.
Title I—Cosmetic Safety
Sec. 101. Registration of cosmetics facilities and cosmetic ingredient statements.
Sec. 102. Review of ingredients and nonfunctional constituents; safety of finished products.
Sec. 103. Good manufacturing practices for cosmetics.
Sec. 104. Adverse event reports.
Sec. 105. Records inspection; mandatory recall authority.
Sec. 106. Labeling and internet sales.
Sec. 107. Consumer information.
Sec. 108. Small businesses.
Sec. 109. Animal testing restrictions.
Sec. 110. Counterfeit cosmetics.
Sec. 111. Foreign supplier verification.
Sec. 112. Applicability with respect to certain cosmetics.
Sec. 113. Saving clause.
Sec. 114. Enforcement.
Title II—Fees Related to Cosmetic Products
Sec. 201. Findings.
Sec. 202. Authority to assess and use cosmetic product fees.
Sec. 203. Direct hiring authority to support activities related to cosmetics.
Sec. 204. Sunset dates.
<enum>I</enum><header>Cosmetic Safety</header>
<section id="H8991D4ACF05D4AD49199CA167018AB19"><enum>101.</enum><header>Registration of cosmetics facilities and cosmetic ingredient statements</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.) is amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="HD674F6D853A946D5880BBA4F1D7B7AF8" style="OLC">
<section id="HA36705695CD7436AB216D94BB07764F7"><enum>604.</enum><header>Definitions</header><text display-inline="no-display-inline">In this chapter:</text> <paragraph id="H54A882678C934106A2B4030D1D33741A"><enum>(1)</enum><header>Animal test</header><text display-inline="yes-display-inline">The term <term>animal test</term> means the internal or external application or exposure of a cosmetic product, cosmetic formulation, or cosmetic ingredient to the skin, eyes, or other body part of a live non-human vertebrate for the purpose of evaluating the safety of a cosmetic product, cosmetic formulation, or cosmetic ingredient.</text>
</paragraph><paragraph id="HF873E561F2384CC5AD2B2063C4B2D4CD"><enum>(2)</enum><header>Contract manufacturer</header><text display-inline="yes-display-inline">The term <term>contract manufacturer</term> means a manufacturer (including the owner, operator, or agent in charge (or any affiliate thereof)) of a cosmetic ingredient, cosmetic formulation, or cosmetic product that does not sell any such cosmetic ingredient, cosmetic formulation, or cosmetic product unless there is a specific contractual agreement in place with respect to that sale.</text>
</paragraph><paragraph id="H305F02E1F9994387ABE17658887F3F3F"><enum>(3)</enum><header>Cosmetic formulation</header><text>The term <term>cosmetic formulation</term> means a preparation of cosmetic raw materials with a qualitatively and quantitatively set composition.</text>
</paragraph><paragraph id="HFA84852152004935950887B6726005D9"><enum>(4)</enum><header>Cosmetic ingredient</header><text display-inline="yes-display-inline">The term <term>cosmetic ingredient</term> means any single chemical entity or mixture used as a component in the manufacture of a finished cosmetic product or cosmetic formulation.</text>
</paragraph><paragraph id="HD8632D8300F445E49E76A1EA35EF0895"><enum>(5)</enum><header>Cosmetic product</header>
<subparagraph commented="no" display-inline="yes-display-inline" id="H9214A1564E784492BDA71CDB631A3509"><enum>(A)</enum><text display-inline="yes-display-inline">The term <term>cosmetic product</term> means a finished cosmetic comprised of a specified set of cosmetic ingredients, which may come in a range of possible amounts for each cosmetic ingredient and which may include a variety of fragrances and colors, and in some specific cosmetic applications, flavors.</text>
</subparagraph><subparagraph id="H139B4531A514488F8C822E1929299A00" indent="up1"><enum>(B)</enum><text display-inline="yes-display-inline">Such term shall include tattoo ink whether or not labeled as a finished cosmetic.</text> </subparagraph></paragraph><paragraph id="H37016745B2EA4309B12F47983DEC009E"><enum>(6)</enum><header>Facility</header><text display-inline="yes-display-inline">The term <term>facility</term> includes any factory, warehouse, or establishment (including a factory, warehouse, or establishment of an importer or of any other entity whose name and address appear on the label of a cosmetic product) that manufactures, processes, packs, or holds cosmetic products or cosmetic formulations. Such term does not include—</text>
<subparagraph id="H97A11B6D5B3C425EAAD9D369986A1E53"><enum>(A)</enum><text display-inline="yes-display-inline">beauty shops and salons that do not otherwise manufacture, process, or package cosmetic products or cosmetic formulations at that location, including beauty stores or counters that offer customized or personalized cosmetic products or cosmetic formulations tailored to individual consumers for sale solely in-person;</text>
</subparagraph><subparagraph id="HC8DABAE3279C47E5B81F9B70633B6A68"><enum>(B)</enum><text display-inline="yes-display-inline">cosmetic product retailers, including individual sales representatives, direct sellers (as defined in <external-xref legal-doc="usc" parsable-cite="usc/26/3508">section 3508</external-xref> of the Internal Revenue Code of 1986), retail distribution facilities, retail franchises, retail warehouses, and pharmacies, that do not otherwise manufacture, process, or package cosmetic products or cosmetic formulations at that location;</text>
</subparagraph><subparagraph id="H4994BE9916724E40A26492FE76EB3C2B"><enum>(C)</enum><text display-inline="yes-display-inline">entities that manufacture or compound cosmetic products solely for use in research, teaching, or pilot plant production and not for sale;</text>
</subparagraph><subparagraph id="HD0F716C460614142BBC87AFA1712AED4"><enum>(D)</enum><text>hospitals, physicians’ offices, and health care clinics;</text> </subparagraph><subparagraph id="H464B40791F9144A18B623B02C5AA2D8A"><enum>(E)</enum><text display-inline="yes-display-inline">hotels, airlines, and other entities that provide complimentary cosmetic products to guests;</text>
</subparagraph><subparagraph id="H6D384D6AEA9146C9A3FA9E69281CBC52"><enum>(F)</enum><text display-inline="yes-display-inline">public health agencies and other nonprofit entities that provide cosmetic products or cosmetic formulations directly to the consumer; or</text>
</subparagraph><subparagraph id="HE37341A64DE54C23AA74B9B9718783F8"><enum>(G)</enum><text>trade shows and other venues where cosmetic product samples are provided free of charge.</text> </subparagraph></paragraph><paragraph id="HCF40A7ECE02F4AC19A55D7195E24A89B"><enum>(7)</enum><header>Foreign facility</header><text display-inline="yes-display-inline">The term <term>foreign facility</term> means a facility that manufactures, processes, packs, or holds, cosmetic products or cosmetic formulations that are exported to the United States without further processing or packaging inside the United States. A cosmetic product or cosmetic formulation is not considered to have undergone further processing or packaging for purposes of this definition solely on the basis that labeling was added or that any similar activity of a de minimis nature was carried out with respect to the cosmetic product or cosmetic formulation.</text>
</paragraph><paragraph id="H371AC846A6BF42D783BF629F3554ECA2"><enum>(8)</enum><header>Nonfunctional constituent</header><text>The term <term>nonfunctional constituent</term> means any substance that is an incidental component of an ingredient, a breakdown product of an ingredient, or a byproduct of the manufacturing process that has not been intentionally added as a separate substance and serves no technical function in the cosmetic product.</text>
</paragraph><paragraph id="H2AFB62F627C64C2D93C5186C6AF8838A"><enum>(9)</enum><header>Professional</header><text display-inline="yes-display-inline">With respect to a cosmetic product, the term <term>professional</term> means—</text> <subparagraph id="H0A5927B758AC4F67A7E6C61C0CF4FDFD"><enum>(A)</enum><text>a dermatologist or other health care professional that administers or provides cosmetic products to patients; or</text>
</subparagraph><subparagraph id="H47FBAD9F8409437BB05A6479A4E0F4B7"><enum>(B)</enum><text>a cosmetologist, nail technician, barber, or esthetician who administers or provides cosmetics within the scope of their business practices.</text>
</subparagraph></paragraph><paragraph id="H4C58B9909F244A78B643D7E5F1E61665"><enum>(10)</enum><header>Professional use</header><text display-inline="yes-display-inline">With respect to a cosmetic product, the term <term>professional use</term> means a preparation of a cosmetic formulation intended only for use by professionals in settings such as cosmetology, nail care, barbering, esthetics, health care, and other professions as determined by the Secretary through regulation.</text>
</paragraph><paragraph id="H92EE409329984E75AAA6C874D9F3100D"><enum>(11)</enum><header>Responsible person</header><text display-inline="yes-display-inline">The term <term>responsible person</term> means the brand owner, operator, or agent in charge who is the domestic or foreign manufacturer, processor, or entity whose name appears on the label of a cosmetic product or a cosmetic formulation distributed in the United States.</text>
</paragraph></section><section commented="no" id="H5942CB84BF7C4E38896BFDA0C660364B"><enum>605.</enum><header>Registration of cosmetic facilities</header>
<subsection commented="no" id="H45A36EA5E31741E98B16B4B4A5592FF3"><enum>(a)</enum><header>Registration for manufacturing and processing facilities</header>
<paragraph commented="no" id="H45AE19E46BC149218B90BB2FE3789E6A"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">The owner, operator, or agent in charge of (or an affiliate thereof) a facility engaged in manufacturing, or processing, of a cosmetic product or a cosmetic formulation distributed in the United States shall register with the Secretary.</text>
</paragraph><paragraph commented="no" id="H468A61B4DAD4466CA9D51EA41FFF3A56"><enum>(2)</enum><header>Electronic registration system</header><text>The Secretary shall—</text> <subparagraph commented="no" id="HE21915F615E64BD792026B9815BF70DD"><enum>(A)</enum><text>maintain an electronic registration system for purposes of this section; and</text>
</subparagraph><subparagraph commented="no" id="H001C90F0CC3E47979B5FBB1CCA72938F"><enum>(B)</enum><text display-inline="yes-display-inline">not later than one year after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, announce that such system is operational.</text> </subparagraph></paragraph><paragraph commented="no" id="HD57F4A69FDC240B29A4DC5CB1FD0F3C3"><enum>(3)</enum><header>Initial registration of existing facilities</header><text display-inline="yes-display-inline">Not later than the date that is 6 months after the date of the announcement required by paragraph (2)(B), each facility engaged in an activity described in paragraph (1) shall be registered under such paragraph.</text>
</paragraph><paragraph commented="no" id="H29D42F6CC4724611978DC413D9B1C72D"><enum>(4)</enum><header>Initial registration of new facilities</header><text display-inline="yes-display-inline">In the case of a facility that first engages in an activity described in paragraph (1) on or after the date that is 18 months after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, such a facility shall register with the Secretary immediately upon engaging in such activity.</text>
</paragraph><paragraph commented="no" id="HE977772DD28248D59F621E19134687A6"><enum>(5)</enum><header>Single registration</header><text>The Secretary shall require only a single registration per registration period for a facility required to be registered under paragraph (1), regardless of whether such facility is manufacturing or processing—</text>
<subparagraph commented="no" id="H38C4D39278404F88B2C06EF387F5FB4E"><enum>(A)</enum><text>its own cosmetic products or cosmetic formulations; or</text> </subparagraph><subparagraph commented="no" id="H8B2035E4F7B844E28C5625E277F954B8"><enum>(B)</enum><text>cosmetic products or cosmetic formulations on behalf of more than one owner, operator, or agent in charge (or affiliate thereof).</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="H30549B2C114F46ED9066E1817E81C4A9"><enum>(b)</enum><header>Registration for packing or holding facilities</header><text display-inline="yes-display-inline">Each facility engaged in packing or holding a cosmetic product or cosmetic formulation distributed in the United States shall register with the Food and Drug Administration. Each such facility shall, not later than 6 months after the Secretary announces the establishment of an electronic registration system for purposes of this section, submit a registration utilizing such system.<italic></italic></text>
</subsection><subsection commented="no" id="H0B45D4999D9843C7A5008308B1248436"><enum>(c)</enum><header>Annual registration renewal</header><text display-inline="yes-display-inline">A facility that continues to engage in any activity that would require registration under subsection (a) or (b) shall submit to the Secretary an annual registration during the first quarter of the fiscal year for which such renewed registration shall be effective.</text>
</subsection><subsection commented="no" display-inline="no-display-inline" id="HCC76FA817A304254BC90D58466D9CFF8"><enum>(d)</enum><header>Fees</header><text display-inline="yes-display-inline">If the average gross annual sales of cosmetic products in the United States of all of the facilities of the responsible person registered under subsection (a)(1) for the previous 3-fiscal-year period is greater than $1,000,000, a registration shall not be complete under this subsection until the responsible person has paid any registration fee required under section 744M.<italic></italic></text>
</subsection><subsection commented="no" id="H56E70000223B41B0ACA6AE668C62374A"><enum>(e)</enum><header>Changes to information</header><text display-inline="yes-display-inline">A facility that submitted a registration under this section shall notify the Secretary of any change to the information required under subsection (a) or (b) not later than 30 days after the date of such change, unless otherwise specified by the Secretary.</text>
</subsection><subsection commented="no" id="H280970C538B340D9923ECBC161499B49"><enum>(f)</enum><header>Format; contents</header>
<paragraph commented="no" id="HDFD6AF7C34C64764AF1BCA019C5569AA"><enum>(1)</enum><header>Electronic format</header><text display-inline="yes-display-inline">Each registration shall be submitted using an electronic format, as specified in a registration form provided by the Secretary.</text>
</paragraph><paragraph commented="no" id="H5E468509D75B4E53AE33EF32EB2B9AEB"><enum>(2)</enum><header>Contents</header><text>The registration shall contain the following information:</text> <subparagraph commented="no" id="H554A39E9BC7B4174AF5481909100FD8E"><enum>(A)</enum><text>Each facility’s name (including any parent company of the facility) and full address, identifying the precise physical location of the facility.</text>
</subparagraph><subparagraph commented="no" id="H515F0240ACE0410B897EE758F03D2578"><enum>(B)</enum><text display-inline="yes-display-inline">The identity of the facility, including the unique facility identifier, if any, previously assigned by the Secretary to the facility under subsection (i).</text>
</subparagraph><subparagraph commented="no" id="H8892A9D7670648D3BB80E65F87468AA3"><enum>(C)</enum><text>All business trading names used by the facility.</text> </subparagraph><subparagraph commented="no" id="H7813D4029CE7463694DAAF370911094E"><enum>(D)</enum><text display-inline="yes-display-inline">The product category (as identified under section 720.4(c) of title 21, Code of Federal Regulations (or any successor regulation)), or other cosmetic categories as determined appropriate by the Secretary (including by guidance) of each cosmetic product or cosmetic formulation manufactured, processed, packed, or held at the facility or on whose label the facility’s name and address appear.</text>
</subparagraph><subparagraph commented="no" id="H725BB47A6A0F462C8F9AE912E1BF38D2"><enum>(E)</enum><text>The type or types of activities conducted at the facility (such as manufacturing, processing, packing, or holding).</text>
</subparagraph><subparagraph commented="no" id="H85E8B6430FF04427BDCB74124BF63641"><enum>(F)</enum><text>The name, title, street address, telephone number, and electronic contact information of the emergency contact for the facility.</text>
</subparagraph><subparagraph commented="no" id="H1A783DF927004495AD9B9207854EB27E"><enum>(G)</enum><text>In the case of a foreign facility, the name, street address, telephone number, emergency contact information for the facility, the name of the United States agent for the facility, and the phone number and electronic contact information of the United States agent.</text>
</subparagraph><subparagraph commented="no" id="H70AD2E065D2C49B4BFCA9354DF167F16"><enum>(H)</enum><text>The name, title, street address, telephone number, and electronic contact information of the individual submitting the registration.</text>
</subparagraph><subparagraph commented="no" id="H0345F5A929854CD48930DD53E998E7E3"><enum>(I)</enum><text>An assurance that the Secretary will be permitted to inspect such facility at the times and in the manner permitted by this Act.</text>
</subparagraph><subparagraph commented="no" id="HB03D7D1934554EAC9EA25EC9600BE7DF"><enum>(J)</enum><text>Additional information pertaining to the facility or to the cosmetic products or cosmetic formulations manufactured, processed, packed, or held at the facility, or on whose label the facility’s name and address appear, including all brand names known to consumers, as the Secretary may require by regulation.</text>
</subparagraph></paragraph><paragraph commented="no" id="HF67BDEA6C1B1412EBDBBEC8E34836AE2"><enum>(3)</enum><header>Abbreviated registration</header><text display-inline="yes-display-inline">The Secretary shall provide for an abbreviated registration renewal process for any facility that has not had any changes to the information submitted by the facility for the preceding registration.</text>
</paragraph></subsection><subsection commented="no" id="HD2B5DFCBE3A44668B10E5EB4373AD305"><enum>(g)</enum><header>Incomplete or inaccurate registration</header>
<paragraph commented="no" id="H2B06329E309C459F960816629105448E"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">Subject to paragraph (2), the Secretary may cancel a registration of a facility under this section if—</text>
<subparagraph commented="no" id="H989FAB416E374B968CF5DD61B256779B"><enum>(A)</enum><text>the Secretary has reasonable grounds to believe that the registration was not properly completed or updated in accordance with this section;</text>
</subparagraph><subparagraph commented="no" id="H72D33A7147D6492493180AA007CCFA57"><enum>(B)</enum><text>a required registration fee has not been paid within 30 days; or</text> </subparagraph><subparagraph commented="no" id="H638DDEA5C1ED419F8B44BD01B95631E2"><enum>(C)</enum><text>the registration otherwise contains false, incomplete, or inaccurate information.</text>
</subparagraph></paragraph><paragraph commented="no" id="HE4F2ECBBC82842C3A1EC5C6464DCF7CE"><enum>(2)</enum><header>Notification</header><text>The Secretary shall, at least 10 days before canceling a registration pursuant to paragraph (1), provide notice to the facility of the intent of the Secretary to cancel such registration that contains the Secretary’s basis for the determination to so cancel the registration.</text>
</paragraph><paragraph commented="no" id="H98FF391817424D4D9C428B05A0DA566D"><enum>(3)</enum><header>Timely update or correction</header><text display-inline="yes-display-inline">If, not later than 7 days after receipt of a notice of intent to cancel under paragraph (2), the facility corrects the registration in accordance with the basis for the cancellation, and the required registration fee, if any, is paid, the Secretary shall not cancel such registration.</text>
</paragraph></subsection><subsection commented="no" id="H0EFA0C211D7F49659ABFA55EA8BA6EC4"><enum>(h)</enum><header>Unique identifier</header><text display-inline="yes-display-inline">At the time of the initial registration of any cosmetic facility under this section, the Secretary shall assign a unique identifier to the facility and provide such identifier to such facility in writing.</text>
</subsection><subsection commented="no" id="HA3DD4FDDAAC04EA396A6D9C4FBD1CDFD"><enum>(i)</enum><header>Registry of facilities</header>
<paragraph commented="no" id="HF2AA3D9A9D724DC88CFD9BF2E33E7CD9"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">The Secretary shall compile, maintain, and update a registry of facilities that are registered under this section, and shall remove from such registry the name of any facility whose registration under this section is cancelled. The registry shall be publicly available.</text>
</paragraph><paragraph commented="no" id="H6A2F2BE3BB8A4581BE7938FA6138E467"><enum>(2)</enum><header>Public availability exceptions</header><text display-inline="yes-display-inline">Information derived from the registry or registration documents that discloses the residential address of an owner, operator, or agent in charge of (or an affiliate thereof) a facility engaged in manufacturing, processing, packing, or holding a cosmetic product or formulation, or a facility owned by such person, or that discloses specific facilities where specific brands of cosmetic products are manufactured or processed shall not be subject to disclosure under section 552 of title 5, United States Code.</text>
</paragraph></subsection></section><section id="HF9658FEE62BC4F6C84A8DC4A86786E37"><enum>606.</enum><header>Cosmetic ingredient statements</header>
<subsection id="H2F14D74A8A89478D8DAC90777FD11AE5"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">For each cosmetic product, the responsible person shall submit to the Secretary a cosmetic ingredient statement, at such time and in such manner as the Secretary may prescribe. The cosmetic ingredient statement shall not become effective until the responsible person pays any applicable fee required under section 744M. <italic></italic></text>
</subsection><subsection id="HCD0C25CC6DD8424797738B4598163F22"><enum>(b)</enum><header>Submission of a cosmetic ingredient statement</header>
<paragraph id="H41AF686A1E164AE58EE6F7C2D4CCE1C2"><enum>(1)</enum><header>Existing cosmetic products</header><text display-inline="yes-display-inline">In the case of a cosmetic product or cosmetic formulation that is marketed on the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, the responsible person shall—</text>
<subparagraph id="H2E07985928F34D369315AC0225F6501F"><enum>(A)</enum><text display-inline="yes-display-inline">not later than the date that is 6 months after the date of the announcement of an electronic registration system required by section 605, submit to the Secretary a cosmetic ingredient statement in accordance with this section; and</text>
</subparagraph><subparagraph id="HB58493D26B7F4F819BC82EF7197AAFF3"><enum>(B)</enum><text>beginning one year after the ingredient statement is submitted under subparagraph (A) and each year thereafter, submit to the Secretary a renewal of such statement, consistent with the requirements in subsection (e), during the first quarter of the fiscal year for which such renewed statement is applicable.</text>
</subparagraph></paragraph><paragraph id="HE04D704815354C10BED37DE32B5260A4"><enum>(2)</enum><header>Cosmetic ingredient statement for new cosmetic products</header>
<subparagraph id="HDAAA79E57C714FDAAC3CD0944574845C"><enum>(A)</enum><header>In general</header><text display-inline="yes-display-inline">Except as provided under subparagraph (B), in the case of a cosmetic product or cosmetic formulation that is first marketed after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title> or a cosmetic product or cosmetic formulation that is reformulated after such date of enactment, the responsible person shall—</text>
<clause id="H30D29980CEED4B4C933824BC47663909"><enum>(i)</enum><text display-inline="yes-display-inline">submit to the Secretary a cosmetic ingredient statement prior to first marketing the new cosmetic product, new cosmetic formulation, or the reformulated cosmetic product or reformulated cosmetic formulation; and</text>
</clause><clause id="HD7166D1070AE43B99ED71E729858CF77"><enum>(ii)</enum><text>beginning one year after the ingredient statement is submitted under clause (i), submit to the Secretary annually thereafter a renewal of such statement during the first quarter of the fiscal year for which the cosmetic ingredient statement is applicable, consistent with the requirements in subsection (e).</text>
</clause></subparagraph><subparagraph id="H761256A7DD5A489E82EA1C3760ECFC46"><enum>(B)</enum><header>Small businesses</header><text display-inline="yes-display-inline">In the case of a responsible person that is a small business, the Secretary shall allow such responsible person to have an additional time period, of a duration to be determined by the Secretary, in which to submit the first cosmetic ingredient statement under subparagraph (A). Such responsible person shall, consistent with the requirements in subsection (e), submit a cosmetic ingredient statement annually thereafter during the first quarter of the applicable fiscal year.</text>
</subparagraph><subparagraph id="H0E69B564A6AC48ED89CC9BE69C4BBD33"><enum>(C)</enum><header>Applicability</header><text>In applying subparagraph (A), a cosmetic product or cosmetic formulation shall not be considered to be first marketed or reformulated after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title> if the only change in such product or formulation is—</text>
<clause id="H0A3EFA1D90C244739FB7D7497ACED5D0"><enum>(i)</enum><text>a change in the amount of an existing ingredient that is previously reported under subsection (c)(2)(E); or</text>
</clause><clause id="H47794D49AB3842B0870A0838D31FF9C0"><enum>(ii)</enum><text>the addition or subtraction of a fragrance, flavor, or color, or such other interchangeable ingredients specified by the Secretary in regulations or guidance, previously reported as a potential ingredient under subsection (c)(2).</text>
</clause></subparagraph></paragraph><paragraph id="H76F5C4CE7A6B4604AE375015B16E4E46"><enum>(3)</enum><header>Abbreviated renewal</header><text>The Secretary shall provide for an abbreviated process for the renewal of any cosmetic ingredient statement under this subsection with respect to which there has been no change since the responsible person submitted the previous statement.</text>
</paragraph></subsection><subsection id="H2AFA77E206AB466EAB8D757A2ED80BD1"><enum>(c)</enum><header>Format; contents</header>
<paragraph id="H163EC89272C14A239200C88451B8D0E3"><enum>(1)</enum><header>Form</header><text>For each cosmetic ingredient statement submitted with respect to a cosmetic product or cosmetic formulation under this section, such statement shall be submitted using an electronic format, in a form specified by the Secretary.</text>
</paragraph><paragraph commented="no" id="H064965E8F3774381A92DDC068C702DB1"><enum>(2)</enum><header>Contents</header><text>Each such cosmetic ingredient statement shall include the following information:</text> <subparagraph commented="no" id="H48A789032AC24F43A17E6CBF5316CCF4"><enum>(A)</enum><text>The unique identifier, assigned under section 605(h), as applicable, of—</text>
<clause commented="no" id="H6576B359FE354D928A04C652D1B68E7A"><enum>(i)</enum><text display-inline="yes-display-inline">the facility or facilities where the cosmetic product or cosmetic formulation is manufactured, processed, packed, or held or, if the same cosmetic product or cosmetic formulation is manufactured, processed, packed, or held in more than one facility, the unique facility identifier of each facility where it is manufactured, processed, packed, or held; and</text>
</clause><clause commented="no" id="H793AB4B2F09F45C78ADF402C7E0006EF"><enum>(ii)</enum><text>the facility whose name and address appear on the label, unless the statement is filed by a contract manufacturer, described in section 604(6)(B).</text>
</clause></subparagraph><subparagraph commented="no" id="H6F8467A79C734EEE83DB4DBC36C4A664"><enum>(B)</enum><text display-inline="yes-display-inline">The brand name and the full name for the cosmetic product or cosmetic formulation as it appears on the label.</text>
</subparagraph><subparagraph commented="no" id="H5EBBE30A42444BC1AA43D0DE3BFFD582"><enum>(C)</enum><text display-inline="yes-display-inline">The listing number, if any, previously assigned by the Secretary under subsection (f) to the cosmetic product or cosmetic formulation.</text>
</subparagraph><subparagraph commented="no" id="H0EE7529C27EB4D6797C94F0CBF6E9862"><enum>(D)</enum><text display-inline="yes-display-inline">The applicable cosmetic category for the cosmetic product or cosmetic formulation.</text> </subparagraph><subparagraph commented="no" id="HE40F1CE0068B428CA2D7F6C148428D5B"><enum>(E)</enum><text display-inline="yes-display-inline">A list of ingredients in the cosmetic product or cosmetic formulation that—</text>
<clause id="H222E19D7017D4320A078355E91D38266"><enum>(i)</enum><text>with respect to each such ingredient, the name adopted in regulations promulgated by the Secretary, if any, or by the common or usual name of the ingredient;</text>
</clause><clause id="H08A9F95D0D124005940BE0AF4BA7C562"><enum>(ii)</enum><text>is consistent with the regulations promulgated by the Food and Drug Administration related to cosmetic labeling requirements; and</text>
</clause><clause commented="no" id="H39DE91BBB6CF49249BC5C916A6A1F79A"><enum>(iii)</enum><text>contains a list of fragrances, flavors, and colors that may be included in the product, interchangeably, which shall include—</text>
<subclause commented="no" id="HD0CE4ACB577F41F0BD7AFCFBBC48E0C8"><enum>(I)</enum><text display-inline="yes-display-inline">in the case of fragrances, each fragrance allergen contained in the cosmetic product as described in section 615, and for fragrances that are purchased from a fragrance supplier, the fragrances shall be identified by the name or code provided by the supplier, and include the name and contact information for the fragrance supplier<italic></italic>; and</text>
</subclause><subclause commented="no" id="H2F0843528C3541E9A30E7A4212D12FAA"><enum>(II)</enum><text>in the case of flavors that are purchased from a flavor supplier, the flavors shall be identified by the name or code provided by the supplier, and include the name and contact information for the flavor supplier;</text>
</subclause></clause><clause commented="no" id="HE0B78F734683465891065BF7F8B0FB82"><enum>(iv)</enum><text>other appropriate interchangeable ingredients as the Secretary may specify in regulations or guidance that may be included in the product; and</text>
</clause><clause commented="no" id="H781BF6EFA1B44E5BA4E721C6F1D7B77B"><enum>(v)</enum><text display-inline="yes-display-inline">in the case of an ingredient (other than a fragrance, flavor, or color) that has been designated for review under section 608, includes potential ranges and amounts of such ingredient.</text>
</clause></subparagraph><subparagraph commented="no" id="HA2BCFFED7FED4FDD9863D0ECBABBF2EC"><enum>(F)</enum><text>The title and full contact information of each individual submitting the statement.</text> </subparagraph><subparagraph commented="no" id="H0779674AEE4B4F2D87F9474327477DB2"><enum>(G)</enum><text>If applicable, information on labeling required under section 614.</text>
</subparagraph><subparagraph commented="no" id="HDE2B3B3C3123493F9780C7735EEBC02C"><enum>(H)</enum><text>Such additional information pertaining to the cosmetic product as the Secretary may require by regulation.</text>
</subparagraph></paragraph><paragraph id="H2BCAEAA808E8477F933DF4BD08568775"><enum>(3)</enum><header>Confidentiality</header><text display-inline="yes-display-inline">Fragrance ingredients included in a cosmetic ingredient statement under paragraph (2)(E), other than fragrance allergens, shall be treated as confidential commercial or trade secret information.</text>
</paragraph><paragraph id="H63FB75F0C7D24F18B68374436E44AF7B"><enum>(4)</enum><header>Contract manufacturing organization facilities</header><text display-inline="yes-display-inline">If a facility manufactures or processes cosmetic products or cosmetic formulations on behalf of an owner, operator, or agent in charge whose name appears on the label of such products or formulations, the Secretary shall require only a single cosmetic ingredient statement for such cosmetic product. Such single cosmetic ingredient statement shall be submitted to the Secretary by the responsible person.</text>
</paragraph><paragraph commented="no" id="H2FD56279747C4DE193F127F0E19D445B"><enum>(5)</enum><header>Cosmetic ingredient statement for certain small businesses</header>
<subparagraph commented="no" id="HBF35D0B9D7E84B169760CECC5DFDA019"><enum>(A)</enum><header>In General</header><text display-inline="yes-display-inline">Notwithstanding any other provision of this subsection, in the case of a responsible person that has had an average of less than $1,000,000 in annual domestic cosmetic sales over the previous 3 years, the Secretary may allow such responsible person—</text>
<clause id="H626E65D9EFD346AFBC194C9A8F8E7DB1"><enum>(i)</enum><text>to submit a simplified cosmetic ingredient statement under this section; and</text> </clause><clause id="H53234DA0F0594425A20AC56E9586AB97"><enum>(ii)</enum><text>an additional time period, of a duration to be determined by the Secretary, in which to submit such simplified cosmetic ingredient statement.</text>
</clause></subparagraph><subparagraph commented="no" id="HEDC2F7C129BC483DAC0575DCBEFFB37B"><enum>(B)</enum><header>Contents</header><text display-inline="yes-display-inline">A responsible person described in subparagraph (A) shall include in each cosmetic ingredient statement submitted under this section, at a minimum—</text>
<clause id="H5620BEF009C2457E8BC6529112F3B532"><enum>(i)</enum><text>a list of ingredients in the cosmetic product or cosmetic formulation, including any fragrance allergens as described in section 615;</text>
</clause><clause id="H4F608B48766342E782B5854F8C7E74C3"><enum>(ii)</enum><text>the applicable cosmetic category for the cosmetic product or cosmetic formulation; and</text> </clause><clause id="HF92C0F43F850415EAFEE1647E4A2D8F2"><enum>(iii)</enum><text>in the case of a cosmetic product or cosmetic formulation that includes a fragrance or flavor purchased from a fragrance or flavor supplier, the contact information for the fragrance or flavor supplier, including the supplier’s name, street address, telephone number, and electronic contact information.</text>
</clause></subparagraph></paragraph></subsection><subsection id="H618D85D4FFEE4FAB9829BBAAB37B4FD3"><enum>(d)</enum><header>Incomplete or inaccurate cosmetic ingredient statement</header>
<paragraph id="HCB8F7671601444F0AC49D0BA3825232E"><enum>(1)</enum><header>In general</header><text>Not earlier than 30 days after providing notice under paragraph (2) and subject to paragraph (3), the Secretary may nullify a cosmetic ingredient statement submitted under this section if the Secretary has reasonable grounds to believe that, except for minor or immaterial errors, the cosmetic ingredient statement was not completed or updated in accordance with this section or otherwise contains false, incomplete, or inaccurate information.</text>
</paragraph><paragraph id="HF7DA6059DE7F4F5C9DE488560FAB2B8C"><enum>(2)</enum><header>Notice of nullification</header><text>If the Secretary nullifies a cosmetic ingredient statement under paragraph (1), the Secretary shall provide to the responsible person submitting such cosmetic ingredient statement under this section notice of any such nullification, including the basis for such nullification.</text>
</paragraph><paragraph id="H29E056BB703F4F77A208EF4461ED891D"><enum>(3)</enum><header>Timely update or correction</header><text display-inline="yes-display-inline">In the case of a cosmetic ingredient statement with respect to which the Secretary has provided notice under paragraph (2), the Secretary shall not nullify such cosmetic ingredient statement if the cosmetic ingredient statement is appropriately updated or corrected not later than 10 days after the date on which such notice is provided.</text>
</paragraph><paragraph id="H96DB645192AB4389A75493CFF399AF18"><enum>(4)</enum><header>Effect of nullification</header><text>No person shall import, export, or otherwise distribute any cosmetic product or cosmetic formulation that is the subject of a cosmetic ingredient statement that is nullified under this subsection.</text>
</paragraph></subsection><subsection id="H2C482A075A00496A9B421AB110D45D94"><enum>(e)</enum><header>Additional requirements</header>
<paragraph id="HC7B48901943F4BD19C94C9C5FE6E3EC7"><enum>(1)</enum><header>Safety requirements</header><text>In submitting a cosmetic ingredient statement for each cosmetic product or cosmetic formulation under this section, a responsible person shall include an attestation that the safety of the product or formulation, including the individual ingredients of such product or formulation, has been substantiated in accordance with section 609.</text>
</paragraph><paragraph commented="no" id="H38AD25B58126401DA401C55992706A12"><enum>(2)</enum><header>Changes to information</header><text display-inline="yes-display-inline">Not later than 90 days after any change to the information required to be in a cosmetic ingredient statement under this section, the responsible person shall notify the Secretary of such change, including the discontinuation of the manufacture of a cosmetic product. Such notification is not required for a change described in subsection (b)(2)(C).</text>
</paragraph></subsection><subsection id="H397F3184D1A948D3BA2125841AAF1B7A"><enum>(f)</enum><header>Cosmetic products list</header>
<paragraph id="H287ABA461E604432A21C2D3E608FD32E"><enum>(1)</enum><header>Listing number</header><text>At the time of the initial submission of any cosmetic ingredient statement under this section, the Secretary shall—</text>
<subparagraph id="H40E8161934064CA5BBE8AA0AD8F1D01E"><enum>(A)</enum><text>assign a unique cosmetic product listing number to the cosmetic ingredient statement; and</text> </subparagraph><subparagraph id="HBE40E7A8A8E843C6A84E829DFF173897"><enum>(B)</enum><text>provide such number to the responsible person who submitted such statement in writing.</text>
</subparagraph></paragraph><paragraph id="HB47A12540CC145E493A6FC45B8B00F83"><enum>(2)</enum><header>Cosmetic products list</header><text>Using cosmetic ingredient statements submitted under this section, the Secretary shall—</text> <subparagraph id="HAA941B76E14A460D8E7BD8DDF5AE5159"><enum>(A)</enum><text>compile and maintain a list of cosmetic products or cosmetic formulations distributed in the United States, including the ingredients of each such product or formulation; and</text>
</subparagraph><subparagraph id="H83A96223543D49D8BB271B63A77DEB31"><enum>(B)</enum><text display-inline="yes-display-inline">upon request of any State, shall make such list available to such State.</text> </subparagraph></paragraph><paragraph commented="no" id="H9492338A3DEE4FE18A474AAD4E1EE09F"><enum>(3)</enum><header>Confidentiality</header><text>Information disclosed to a State that is exempt from disclosure under section 552(b)(4) of title 5, United States Code, shall be treated as a trade secret and confidential information by the State. Such State and its employees in possession of such information shall be subject to the same laws governing information disclosure as employees of the Food and Drug Administration.</text>
</paragraph></subsection><subsection id="H48EC0ED0CECF46488930DD4EEA188792"><enum>(g)</enum><header>Exemption</header><text display-inline="yes-display-inline">A responsible person shall be exempt from the requirements of this section if such person has had an average of less than $500,000 in annual domestic cosmetic product sales over the previous three years. Such exemption shall not apply to cosmetic products that are intended to be injected under the skin or into the eye, including tattoo ink, or ingredients selected by the Food and Drug Administration for review under section 608 if such ingredient is included in a cosmetic product or cosmetic formulation distributed by such person described.</text>
</subsection></section><section id="HABBFABF219454B459760D43C077C1E4A"><enum>607.</enum><header>Suspension of registration or cosmetic ingredient statement</header>
<subsection id="H0D53A8896857445CB0D676F5C206F791"><enum>(a)</enum><header>Suspension of registration of a facility</header><text display-inline="yes-display-inline">If the Secretary determines that a cosmetic product or cosmetic formulation manufactured, processed, packed, or held by a facility registered under section 605 has a reasonable probability of causing serious adverse health consequences or death to humans, the Secretary may suspend the registration of such facility.</text>
</subsection><subsection id="H9D8B7A0BD08D46288DBB4A52AB6010BB"><enum>(b)</enum><header>Suspension of cosmetic ingredient statement</header><text display-inline="yes-display-inline">If the Secretary determines that a cosmetic product or cosmetic formulation manufactured in a registered facility has a reasonable probability of causing serious adverse health consequences or death to humans, the Secretary may suspend the cosmetic ingredient statement of that product or formulation.</text>
</subsection><subsection id="H561AF65906C1426AB2772F7ADD440259"><enum>(c)</enum><header>Notice of suspension</header><text>Before suspending the registration of a facility or a cosmetic ingredient statement<italic></italic> under this section, the Secretary shall provide—</text> <paragraph id="H83CE0499D6844A989798D223D484BE9C"><enum>(1)</enum><text>notice to the facility or responsible person, as appropriate, of the intent to suspend such registration or the cosmetic ingredient statement<italic></italic>, which shall specify the basis of the determination by the Secretary for that suspension; and</text>
</paragraph><paragraph id="H72B1FC31881C4E94B034BB719540C23B"><enum>(2)</enum><text>an opportunity, within 2 business days of the notice provided under paragraph (1), for the facility or responsible person that is the subject of such notice, as appropriate, to address the reasons for possible suspension of the registration of the facility or cosmetic ingredient statement.</text>
</paragraph></subsection><subsection id="H3F88B2A7036641FC83A8644BDFD7694E"><enum>(d)</enum><header>Reinstatement</header><text>Upon a determination by the Secretary that adequate grounds do not exist to continue the suspension actions under subsection (a) or (b), the Secretary shall promptly vacate the suspension and reinstate the registration of the facility or the cosmetic ingredient statement.<italic></italic></text>
</subsection><subsection id="H21AE9FC2D63B4EDC960B42A31502BDF9"><enum>(e)</enum><header>Effect of suspension</header><text display-inline="yes-display-inline">If the registration of a facility is suspended under this section, no person shall import or export cosmetics or otherwise distribute cosmetic products or cosmetic formulations from such facility.</text>
</subsection><subsection id="H47B027D6B7074CEAAD5D54F723E696D7"><enum>(f)</enum><header>No delegation</header><text>The authority conferred by this section to issue an order to suspend a registration or vacate an order of suspension shall not be delegated to any officer or employee other than the Commissioner.</text></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section id="HA4B15AEB84F84AE1B47E46EB29B861A9"><enum>102.</enum><header>Review of ingredients and nonfunctional constituents; safety of finished products</header>
<subsection id="H5210337FBD50467EAEF9D9A3C03732EF"><enum>(a)</enum><header>Amendments</header><text display-inline="yes-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 101, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H906F03A434A34CEB92EACE25B6F023E8" style="OLC">
<section id="H742E1D6FDC23434AA9410963BF816DE3"><enum>608.</enum><header>Review of ingredients and nonfunctional constituents</header>
<subsection id="HF59B7240D18149E9B6F1D0255DDBB79D"><enum>(a)</enum><header>Ingredients and nonfunctional constituents subject To review</header>
<paragraph id="H5C00A060C1074971904733AA63468B98"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">Not later than 3 years after the date of the enactment of the Cosmetic Safety Enhancement Act of 2019, the Secretary shall review the safety of cosmetic ingredients or nonfunctional constituents (or categories thereof). Upon the completion of such review, the Secretary shall issue an order under subsection (d) with respect to the use of each such ingredient (or a category thereof) and presence of each such nonfunctional constituent in cosmetic products or cosmetic formulations (or a category thereof).</text>
</paragraph><paragraph id="HEE196D99366C4283A1D042B8B67EC808"><enum>(2)</enum><header>Ingredients and nonfunctional constituents to be reviewed</header><text display-inline="yes-display-inline">The Secretary shall select and complete a review, on an ongoing basis, of cosmetic ingredients or nonfunctional constituents that were not reviewed in the prior 3 years. Such ingredients or nonfunctional constituents, including any classes of ingredients or nonfunctional constituents, should be selected after consultation with stakeholders, including industry and consumer groups.</text>
</paragraph><paragraph id="H20EFC8FE165445EB9E6B61CA6E0F70CB"><enum>(3)</enum><header>Process for review</header><text display-inline="yes-display-inline">The Secretary shall—</text> <subparagraph id="HCBC4803DD2EC40F4959CD8AE78E0A370"><enum>(A)</enum><text>publish in the Federal Register a list of the ingredients, nonfunctional constituents (or categories thereof) identified for review under paragraph (2); and</text>
</subparagraph><subparagraph id="H96E9D405FF6D402980EF5805A84E1114"><enum>(B)</enum><text display-inline="yes-display-inline">open a public docket to solicit public input and data relevant to the safety of the ingredients, nonfunctional constituents (or classes or categories thereof) so listed for a period of not less than 60 days.</text>
</subparagraph></paragraph><paragraph id="H8EDAF7E1FC3B4B4F89EC79EA92B662B4"><enum>(4)</enum><header>Public comment</header><text display-inline="yes-display-inline">Comments may be submitted to the Secretary at any time with respect to the safety of cosmetic ingredients or nonfunctional constituents (or categories thereof), regardless of whether such ingredients or constituents (or categories thereof) have been selected for review under this subsection.</text>
</paragraph></subsection><subsection id="H666009AE9F2741DCBA3932ECF3ADE33F"><enum>(b)</enum><header>Reviewed ingredients and nonfunctional constituents</header><text display-inline="yes-display-inline">The Secretary shall maintain a list, posted on the internet website of the Food and Drug Administration, of each cosmetic ingredient, nonfunctional constituent, and category of ingredients or nonfunctional constituents for which final orders have been issued under subsection (d)(3), and with respect to each such ingredient or nonfunctional constituent—</text>
<paragraph id="HD3B6B448CB0E4A8DBD30F5FBAE452B48"><enum>(1)</enum><text display-inline="yes-display-inline">the finding made for each such ingredient, nonfunctional constituent, or category under subsection (d)(4), as modified by any order under subsection (e); and</text>
</paragraph><paragraph id="HBC9430B2EEDA4F37BACB313F923171DA"><enum>(2)</enum><text>if applicable, compliance dates that are the subject of a final order under subsection (d)(3).</text> </paragraph></subsection><subsection id="HB02D8671606C4A2DB565FC07E5CA664D"><enum>(c)</enum><header>Initiative of the FDA</header><text>The Secretary may, at any time, propose the issuance of an order on the safety of a cosmetic ingredient or nonfunctional constituent (or category thereof) that was not previously listed pursuant to subsection (a).</text>
</subsection><subsection id="HA2F5DBAD999945B1996D741614899AD6"><enum>(d)</enum><header>Determination on safety</header>
<paragraph id="H7C1299BCB30C4197A3D4BD9326D4E305"><enum>(1)</enum><header>Proposed administrative order</header><text display-inline="yes-display-inline">Following consideration of data and comments to the public docket opened under subsection (a)(3) and any other information before the Secretary with respect to the safety of a cosmetic ingredient or nonfunctional constituent (or category thereof), the Secretary shall—</text>
<subparagraph id="H954AA5161ED948BAAC779ABFE9E28368"><enum>(A)</enum><text>determine whether there is adequate evidence to make an initial finding for purposes of making a determination described in paragraph (4);</text>
</subparagraph><subparagraph id="H3F18A2123F07479EA88D2AE9E6DAF8FE"><enum>(B)</enum><text display-inline="yes-display-inline">if the Secretary determines that there is adequate evidence to make such a finding, issue a proposed administrative order containing the Secretary’s initial determination on the safety of such ingredient or nonfunctional constituent (or category thereof) as described in paragraph (4) and shall post such order on the internet website of the Food and Drug Administration, notwithstanding subchapter II of <external-xref legal-doc="usc-chapter" parsable-cite="usc-chapter/5/5">chapter 5</external-xref> of title 5, United States Code; and</text>
</subparagraph><subparagraph id="HD0F6899CE96F48D4A80E9ECA85AC41B5"><enum>(C)</enum><text>in the case of a proposed administrative order in which the Secretary makes a determination described in subparagraph (B) or (C) of paragraph (4), include in such order a compliance date<italic></italic>.</text>
</subparagraph></paragraph><paragraph id="H392239CEF84D4FA9826B89EAAF71A3BA"><enum>(2)</enum><header>Public comment</header><text display-inline="yes-display-inline">The Secretary shall open a public docket for the submission of public comments (including comments on whether any proposed compliance date included in such order is feasible)—</text>
<subparagraph id="H57E22F6FA50F4FAE96F45E1D4EFC538A"><enum>(A)</enum><text>in the case of a proposed administrative order under paragraph (1), for a period of not less than 60 days, beginning on the date of the issuance of the order; or</text>
</subparagraph><subparagraph id="HE1129EC5B38B4519B3CA1AA77DC68082"><enum>(B)</enum><text>in the case of a final administrative order under paragraph (3), for a period of not less than 60 days, beginning on the date that is at least 60 days before the effective date of the order.</text>
</subparagraph></paragraph><paragraph id="H892C254805EC421BA2CAEE1E38223D98"><enum>(3)</enum><header>Final administrative order</header><text display-inline="yes-display-inline">Following the public comment period under paragraph (2) and consideration of comments to the public docket under such paragraph and any other information before the Secretary, the Secretary shall—</text>
<subparagraph id="H4EF8D15D20B44E989D5E5C6E6C9ED7B3"><enum>(A)</enum><text display-inline="yes-display-inline">determine whether there is adequate evidence to make an initial finding for purposes of making a determination described in paragraph (4);</text>
</subparagraph><subparagraph id="H5EE31E19DB5B443084EF09BE2B757375"><enum>(B)</enum><text display-inline="yes-display-inline">if the Secretary determines that there is adequate evidence to make such a final finding, the Secretary shall issue a final administrative order and shall post such order on the internet website of the Food and Drug Administration, notwithstanding subchapter II of <external-xref legal-doc="usc-chapter" parsable-cite="usc-chapter/5/5">chapter 5</external-xref> of title 5, United States Code; and</text>
</subparagraph><subparagraph id="H8B5BA5D3F707415E8295E40EAA2554BA"><enum>(C)</enum><text display-inline="yes-display-inline">in the case of a final administrative order in which the Secretary makes the determination described in subparagraph (B) or (C) of paragraph (4), include in such order a compliance date. <italic></italic></text>
</subparagraph></paragraph><paragraph id="H9AF8E6B2228E4FDAAE965EB28F52F4C6"><enum>(4)</enum><header>Determinations</header><text>In a proposed administrative order issued under paragraph (1) or a final administrative order issued under paragraph (3), as applicable, the Secretary shall make a determination that the ingredient or nonfunctional constituent is—</text>
<subparagraph id="H765703CDBCD849548A834267463A2D4E"><enum>(A)</enum><text>safe in cosmetic products without the need for specified conditions of use or tolerances;</text> </subparagraph><subparagraph id="H96E5E017D8F74C9F9939D923DF9860CD"><enum>(B)</enum><text>safe in cosmetic products under specified conditions of use or tolerances; or</text>
</subparagraph><subparagraph id="HE8FA9351E7AD4AE980055E5CBDC9B9B9"><enum>(C)</enum><text>not safe in cosmetic products.</text> </subparagraph></paragraph><paragraph id="H4010328325A640EC88643E70D16B8EFF"><enum>(5)</enum><header>Conditions of use and tolerances</header><text>An order under paragraph (4)(B) shall include such conditions on the use of an ingredient or such tolerances on the presence of a nonfunctional constituent (or category thereof) as are necessary for the safety of cosmetic products containing such ingredient or nonfunctional constituent (or category thereof), including—</text>
<subparagraph id="HE7E8A539ED5341D2A8FE0F4BA56629EE"><enum>(A)</enum><text display-inline="yes-display-inline">limits on the amount or concentration of the ingredient or nonfunctional constituent (or category thereof) that may be present in a cosmetic product, including limits in products intended for children, pregnant women, and other vulnerable populations, and limits on use near the eye or mucosal membranes;</text>
</subparagraph><subparagraph id="H95379AB9E3754AFCBF9B910427F82E0A"><enum>(B)</enum><text>warnings that are necessary or appropriate under section 614, including warnings related to use by children, pregnant women, populations with high exposure to the ingredient (such as workers who are exposed through production practices or handling of final products), or other vulnerable populations, to help ensure safe use of cosmetic products containing the ingredient or nonfunctional constituent (or a category thereof); and</text>
</subparagraph><subparagraph id="HD6D6D4058EBB4650AAB3CAD090D24046"><enum>(C)</enum><text>such other conditions as are necessary for the safety of cosmetic products containing such ingredient or nonfunctional constituent (or category thereof).</text>
</subparagraph></paragraph><paragraph id="H04C5F6D3E1AB4EBB9AA855B43D650278"><enum>(6)</enum><header>Contents of order</header><text display-inline="yes-display-inline">A final administrative order under this subsection shall—</text> <subparagraph id="H87360C9A667443FA95B446113788A05A"><enum>(A)</enum><text>set forth the determination of the Secretary on safety;</text>
</subparagraph><subparagraph id="HCE3942C45D4B452680E192D61FCFB3F3"><enum>(B)</enum><text>include a summary of the valid scientific evidence supporting the determination;</text> </subparagraph><subparagraph id="H094C3EE33B9B47E2B86A1B9AA683E9E1"><enum>(C)</enum><text>include any conditions of use or tolerances under paragraph (4)<italic></italic>(B); and</text>
</subparagraph><subparagraph id="H9A5A29774F074204B47B1A9474B5740F"><enum>(D)</enum><text>be effective upon its publication on the internet website of the Food and Drug Administration and shall be considered final agency action unless a later compliance date is otherwise specified.</text>
</subparagraph></paragraph></subsection><subsection id="HF1A3924157E64EDEA0FB06E4979D4F53"><enum>(e)</enum><header>Modification of an order</header><text>An order issued under subsection (d) may be modified or revoked by the Secretary on the initiative of the Secretary or in response to a petition.</text>
</subsection><subsection commented="no" id="H75C8D3FAD72348DF874E88797B138E18"><enum>(f)</enum><header>Inadequate evidence</header>
<paragraph commented="no" id="HE3B74830E7D94381B827036EEA38DED4"><enum>(1)</enum><header>Notice; Extension</header><text>If the Secretary determines that available data and information are not adequate to make a proposed or final determination under subsection (d), with respect to the safety of a cosmetic ingredient or nonfunctional constituent (or a category thereof), the Secretary shall—</text>
<subparagraph commented="no" id="HB1BC84F9E73D4C8C98BEBF73FAEE4310"><enum>(A)</enum><text>publish such determination on the internet website of the Food and Drug Administration not later than 180 days after the close of the relevant comment period for the ingredient or nonfunctional constituent (or category thereof) under paragraph (2) or (3) of subsection (d), as applicable; and</text>
</subparagraph><subparagraph commented="no" id="HDC38A77E976F447C82E1E8D2E113E3C5"><enum>(B)</enum><text display-inline="yes-display-inline">include in such publication a notice providing interested persons an additional 30 days from the date on which the notice is published to provide additional data and information and an opportunity for a meeting pursuant to paragraph (2).</text>
</subparagraph></paragraph><paragraph commented="no" id="HB6A9A8F19CBC4253A51BBC3936A26ED8"><enum>(2)</enum><header>Meetings</header><text display-inline="yes-display-inline">The Secretary may offer a responsible person of such cosmetic ingredient or nonfunctional constituent (or category thereof) a confidential meeting with respect to a finding under paragraph (1), to discuss matters relating to the data and information requirements to support a determination of safety of such ingredient or nonfunctional constituent (or category thereof), which may involve confidential information. Such meeting should be convened in a reasonable time period agreed upon between the responsible person and the Secretary.</text>
</paragraph><paragraph commented="no" id="HE4CB77617E75456C842A8CC90854F072"><enum>(3)</enum><header>Determination; Order</header>
<subparagraph commented="no" id="H677C33CCC77E4F6F850D294E53AA483B"><enum>(A)</enum><header>Inadequate data and information</header><text>If the Secretary determines that the available data and information are not adequate to make a proposed or final determination under subsection (d) with respect to the safety of a cosmetic ingredient or nonfunctional constituent (or category thereof), the Secretary shall—</text>
<clause commented="no" id="HADAB11756896402D88D51761511A1BE8"><enum>(i)</enum><text display-inline="yes-display-inline">publish such finding on the internet website of the Food and Drug Administration not later than 180 days after the close of the relevant comment period for the ingredient or nonfunctional constituent (or category thereof) under paragraph (2) or (3) of subsection (d), as applicable; and</text>
</clause><clause commented="no" id="H688B087D484F452988B8C7D4298E12F2"><enum>(ii)</enum><text display-inline="yes-display-inline">include in such publication a notice providing interested persons an additional 30 days from the date on which the notice is published to provide additional data and information and an opportunity for a meeting pursuant to paragraph (2).</text>
</clause></subparagraph><subparagraph commented="no" id="HF462DB94B62A48148A6629C42DA4CABB"><enum>(B)</enum><header>Adequate data and information</header><text display-inline="yes-display-inline">If the Secretary determines, after considering any additional data and information submitted pursuant to paragraph (1)(B), that the available data and information are adequate to make a determination with respect to the safety of a cosmetic ingredient or nonfunctional constituent (or category thereof), the Secretary shall—</text>
<clause id="HAA05C1FFEEB24901B643140005E5841D"><enum>(i)</enum><text display-inline="yes-display-inline">in the case of a determination described in subparagraph (A) of subsection (d)(4), within 180 days of the close of the applicable comment period under subsection (d)(2), issue a final administrative order, with respect to such cosmetic ingredient or nonfunctional constituent (or category thereof), in accordance with subsection (d)(3);</text>
</clause><clause id="H2B3DB6FFCD8148F6B4AD1E9B9FF1814B"><enum>(ii)</enum><text>in the case of a determination described in subparagraph (B) of subsection (d)(4), within 180 days of the close of the applicable comment period under subsection (d)(2), issue a proposed administrative order, followed by a final administrative order, with respect to such cosmetic ingredient or nonfunctional constituent (or category thereof), in accordance with subsection (d)(3); and</text>
</clause><clause id="HCB7CF78A806045EB9679194D7CC5DF49"><enum>(iii)</enum><text display-inline="yes-display-inline">in the case of a determination described in subparagraph (C) of subsection (d)(4), within 180 days of the close of the applicable comment period under subsection (d)(2), issue a final administrative order, with respect to such cosmetic ingredient or nonfunctional constituent (or category thereof), in accordance with subsection (d)(3) specifying the date by which sale of such ingredient or nonfunctional constituent must cease.</text>
</clause></subparagraph></paragraph></subsection><subsection commented="no" id="HE71B380D1A314608800AEC452248F82F"><enum>(g)</enum><header>Safety assessment standards</header>
<paragraph commented="no" id="H99269496EDB8477F96E3E0D26117D3DD"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">In assessing the safety of an ingredient or nonfunctional constituent (or category thereof) under this section, the Secretary shall consider—</text>
<subparagraph commented="no" id="HA89FB2B846EA46B8AF0D4486E585D763"><enum>(A)</enum><text>whether there is adequate evidence to support a reasonable certainty among competent scientists that—</text>
<clause commented="no" id="H5467A5E8D9E941AD8BF79CD4140AF2B1"><enum>(i)</enum><text>in the case of a cosmetic ingredient, the ingredient is not harmful under the recommended or suggested conditions of use or customary or usual use; or</text>
</clause><clause commented="no" id="H30DD4ABCBEAE452EA6E4A1BECFF3CA43"><enum>(ii)</enum><text>in the case of a nonfunctional constituent, that the nonfunctional constituent is not harmful under the recommended or suggested tolerance levels or the level at which it is customarily or usually present;</text>
</clause></subparagraph><subparagraph commented="no" id="H32E406649AF64C31BDA9E25F2B9BAD36"><enum>(B)</enum><text display-inline="yes-display-inline">the probable human exposure to the ingredient or nonfunctional constituent (or category thereof) from expected use in cosmetic products and cosmetic formulations;</text>
</subparagraph><subparagraph commented="no" id="H94A98E63C89F438B867D38E7B438B830"><enum>(C)</enum><text display-inline="yes-display-inline">the probable cumulative and aggregate effect in humans of relevant exposure to the ingredient or nonfunctional constituent (or category thereof) or to any chemically or pharmacologically related substances from use in cosmetics or other products with similar routes of exposure under recommended or suggested conditions of use or their customary use, to the extent adequate data are available for analysis, and if appropriate, available information on the total exposure to a cosmetic ingredient or nonfunctional constituent from all sources; and</text>
</subparagraph><subparagraph commented="no" id="HF99CAFDFA2EC4E9FA89C80D0B6D0FA6E"><enum>(D)</enum><text display-inline="yes-display-inline">whether warnings or recommendations in a cosmetic product label, as part of any conditions of use or tolerances imposed by the Secretary in a determination described in subparagraph (B) of subsection (d)(4), would be necessary and appropriate to help ensure the safety of the ingredient or nonfunctional constituent (or category thereof).</text>
</subparagraph></paragraph><paragraph commented="no" id="HCCED6FA8F6BB4FBDA2D4449DDF6ACFB1"><enum>(2)</enum><header>Minor adverse reactions</header><text>The Secretary may not consider a cosmetic ingredient or nonfunctional constituent (or category thereof) harmful under paragraph (1) solely because it can cause minor adverse health reactions, such as minor transient allergic reactions or minor transient skin irritations, in some users.</text>
</paragraph><paragraph commented="no" id="H2251020A2F7945129EAC870525F648D3"><enum>(3)</enum><header>Data and information</header>
<subparagraph commented="no" id="HEAADF363496C43B78BDBAC611D30CB03"><enum>(A)</enum><header>Required information</header><text>A determination that a cosmetic ingredient or nonfunctional constituent (or category thereof) is safe in cosmetics under this section shall be based upon adequate evidence submitted or otherwise known to the Secretary, which shall include full reports of all available studies, published or unpublished, that are adequately designed to show whether the ingredient or nonfunctional constituent is safe. Such studies may include in vitro and in silico studies and epidemiological studies, biomonitoring studies, and studies focused on various points during the lifespan of the subject, that use scientifically valid methodology.</text>
</subparagraph><subparagraph commented="no" id="HCCEC111E6A664B7DB89A1458305A898A"><enum>(B)</enum><header>Additional relevant information</header><text>The Secretary shall consider any other relevant information related to the safety of a cosmetic ingredient or nonfunctional constituent (or category thereof), including—</text>
<clause commented="no" id="H2B09F69F5D7C4C5D8FC85EAC4C55F65A"><enum>(i)</enum><text>adverse event reports;</text> </clause><clause commented="no" id="H2B31508CE3CC4186868B9B29167167F4"><enum>(ii)</enum><text>findings and information from State, Federal, national, and international entities and other bodies composed of scientific and medical experts;</text>
</clause><clause commented="no" id="HF2F9C92BAEAE440E9BEAF7839F8FA0A1"><enum>(iii)</enum><text>if the ingredient or nonfunctional constituent (or category thereof) is lawfully used or present in other products regulated by the Secretary, the scientific basis for such use; and</text>
</clause><clause commented="no" id="HA3A30FAAFE9E437989E29644DA891790"><enum>(iv)</enum><text>experience with the ingredient or nonfunctional constituent (or category thereof) in products that are distributed in the United States or in other countries, if such experience is well-documented and has resulted in substantial human exposure to the ingredient or nonfunctional constituent over time.</text>
</clause></subparagraph></paragraph></subsection><subsection commented="no" id="HD9D24AAA562848868AFEEC670BF3623C"><enum>(h)</enum><header>Coal tar hair dye</header><text display-inline="yes-display-inline">In assessing for purposes of this section the safety of coal tar hair dye or any ingredient or nonfunctional constituent therein, the Secretary shall not make a determination that the dye, ingredient, or nonfunctional constituent is not safe for use in cosmetic products solely because the dye, ingredient, or nonfunctional constituent can cause allergic reactions.</text>
</subsection></section><section commented="no" id="H40D6059E5CEA45DDA1B410C0FF4C4307"><enum>609.</enum><header>Safety of finished cosmetic products</header>
<subsection commented="no" id="HD6FE3931A84840D9B032EE18659791E3"><enum>(a)</enum><header>Determination</header>
<paragraph commented="no" id="HA0E77D74F21B4BD382407E7FC6BB6D81"><enum>(1)</enum><header>In general</header><text>Each responsible person for a finished cosmetic product shall, before first distributing the product for sale, make a written determination that the product is safe under the conditions of use recommended in the labeling of the product. Such determination shall be based on adequate evidence that—</text>
<subparagraph id="H0D785DD161964EB3B5B419AE3060BED8"><enum>(A)</enum><text>each ingredient in the finished product is safe for the use recommended or suggested in the labeling of the product and for the customary or usual use of the product; and</text>
</subparagraph><subparagraph id="HDFEECE97A8FD45228D5FC8358607D934"><enum>(B)</enum><text>the finished product is safe.</text> </subparagraph></paragraph><paragraph commented="no" id="HE075778BD7834408B1B1CF27346F6D8A"><enum>(2)</enum><header>New information</header><text>If new information relevant to the determination becomes available, the responsible person shall promptly update the determination to address that information. <italic></italic></text>
</paragraph></subsection><subsection commented="no" id="H2D02C06D6DB64278BFA1CD35A9010756"><enum>(b)</enum><header>Presumption of adequate evidence</header>
<paragraph commented="no" id="H8BDE673A0DE34E77AA092CFC04023515"><enum>(1)</enum><header>In general</header><text>Except as provided in subsection (c), a determination made under subsection (a) with respect to a finished cosmetic product shall be presumed to be based on adequate evidence if it is supported by—</text>
<subparagraph commented="no" id="H639D2C88E3FF4982921847352859CA94"><enum>(A)</enum><text>with respect to each ingredient in the finished cosmetic product—</text> <clause commented="no" id="HED54992B392C4B50A64D5B302A7926DA"><enum>(i)</enum><text>references to an official statement by one or more expert medical or scientific bodies that the ingredient is safe under the conditions of use recommended or suggested in the product’s labeling or under such conditions of use as are customary or usual; or</text>
</clause><clause commented="no" id="H40CF3F4B4D2E4FDAB56F3C631D600A08"><enum>(ii)</enum><text>appropriate safety testing of the ingredient; and</text> </clause></subparagraph><subparagraph commented="no" id="HAA55FEB6146248BCB477279983C0AE7E"><enum>(B)</enum><text>appropriate safety substantiation of the finished cosmetic product beyond the safety substantiation of individual ingredients and consideration of the combination of ingredients.</text>
</subparagraph></paragraph><paragraph commented="no" id="H488F2091168647288504C34FEE75A06B"><enum>(2)</enum><header>Statement of an expert medical or scientific body</header><text>For purposes of applying paragraph (1)(A)(i), a statement of an expert medical or scientific body is an official statement of that body, if—</text>
<subparagraph commented="no" id="H9FA74FD8312142BD86B518786A3C4B0F"><enum>(A)</enum><text>the medical or scientific body is a Federal, State, national, or international entity with recognized expertise in chemical or cosmetic safety, or other similarly recognized body composed of scientific and medical experts;</text>
</subparagraph><subparagraph commented="no" id="H708E8F6977C64ADFA1916E79C2CFE3AF"><enum>(B)</enum><text>the statement is based upon adequate data to support the finding of safety, and such data are available to the Secretary; and</text>
</subparagraph><subparagraph commented="no" id="H19FE3F46890F40B1974356A8F3644E0F"><enum>(C)</enum><text>the statement is published and endorsed by the medical or scientific body and is not a statement of an employee of such body made in the individual capacity of the employee.</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="H8F3CBE3AF0464F749CBFB311F59E0C67"><enum>(c)</enum><header>Rebuttal of presumption</header><text><italic></italic>Notwithstanding subsection (b), a determination under subsection (a) will not be presumed to be based on adequate evidence if—</text>
<paragraph commented="no" id="H8EBB4825FA6244C39AD3695BA20A2B90"><enum>(1)</enum><text>the Secretary issues an order under section 608 that an ingredient or nonfunctional constituent in the finished product is not safe under the product’s conditions of use or customary or usual use; or</text>
</paragraph><paragraph commented="no" id="HEBC592C7272C488F8F30E3424098B38C"><enum>(2)</enum><text>the Secretary has provided the manufacturer with notice that—</text> <subparagraph commented="no" id="H41A57B3D7A2546769160BE9EE2D93E2D"><enum>(A)</enum><text>the manufacturer has not met the criteria under subsection (b); or</text>
</subparagraph><subparagraph commented="no" id="HBE011C681A964A749B54B6101FDEDCC8"><enum>(B)</enum><text>the Secretary has information that raises significant questions about the safety of the product or any of its ingredients.</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="H8C457577EA9D447F86F1F8DDBFC74BA8"><enum>(d)</enum><header>Timely update</header><text>Upon notice of inadequate evidence under subsection (c), the responsible person shall have 10 days to submit additional evidence to the Secretary regarding the safety of an ingredient, nonfunctional constituent, or the entire cosmetic product, and the Secretary shall have 30 days from the date of receipt of such additional evidence to provide the responsible person with notice that the criteria under subsection (b) have been met or not met.</text>
</subsection><subsection commented="no" id="HF74D21D794744F7592B86F157ED79F4E"><enum>(e)</enum><header>Records maintenance</header><text>The responsible person shall maintain records documenting the determination required under this section and the information on which it is based until 5 years after the finished product is no longer marketed.</text>
</subsection><subsection commented="no" id="H01C306A03B0D4649ADE062EA2EFEBDCE"><enum>(f)</enum><header>Submission of records</header>
<paragraph commented="no" id="HFDDCF7C0B1F24B4A8A6703CEA1C7D632"><enum>(1)</enum><header>In general</header><text>The records required under subsection (e) shall, upon the written request of the Secretary to the responsible person, be provided to the Secretary within a reasonable timeframe not to exceed 30 days, in electronic form.</text>
</paragraph><paragraph commented="no" id="HD338626E88F84B0180D14FD2C0E48533"><enum>(2)</enum><header>Criteria</header><text>The Secretary may require records under paragraph (1) if—</text> <subparagraph commented="no" id="H90E84194FA274CD2BE55AC5CDE0E9F8E"><enum>(A)</enum><text>the Secretary has a reasonable belief, described in written notice, that—</text>
<clause commented="no" id="HB9ADD945C82A4339AE63B416DDC5E6AD"><enum>(i)</enum><text>the finished product may be harmful based on adverse event reports or other scientific information;</text> </clause><clause commented="no" id="HB4EC9B9C391B48EE960998277C6A1EFE"><enum>(ii)</enum><text>scientific information raises credible and relevant questions about the safety of the product or any of its ingredients;</text>
</clause><clause commented="no" id="HDA9D976C05264C74ACB3FAA530552F54"><enum>(iii)</enum><text display-inline="yes-display-inline">the determination required under subsection (a) is not supported by adequate evidence; or</text> </clause><clause commented="no" id="HF10960FFCBA34AB7A272E43F7DF4137E"><enum>(iv)</enum><text>one or more of the criteria to establish a presumption of adequate evidence of safety in subsection (b) has not been satisfied;</text>
</clause></subparagraph><subparagraph commented="no" id="H72CA19539B924148B1474C84F2364823"><enum>(B)</enum><text>the Secretary, an expert regulatory body, or an expert body composed of scientific and medical experts finds an ingredient in the product to be unsafe under the conditions of use of the product; or</text>
</subparagraph><subparagraph commented="no" id="H39BBBFD005544286975DC7790EF783C5"><enum>(C)</enum><text>the Secretary concludes that submission of the records will serve the public health or otherwise enable the Secretary to fulfill the cosmetic safety purposes of this section.</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="HED25DE1308E441FFA67FD074DC540E42"><enum>(g)</enum><header>Guidance and regulations</header>
<paragraph commented="no" id="H58A38E4C7D324DFCAD9C2BB6020279EC"><enum>(1)</enum><header>In general</header><text>The Secretary shall issue guidance describing the evidence necessary to support a determination under subsection (a), and may, by regulation, establish exemptions to the requirements of this section, if the Secretary determines that such exemptions are supported by adequate evidence and would have no adverse effect on public health.</text>
</paragraph><paragraph commented="no" id="H5B0643CFFD5A45FFB348E8EB520F58D3"><enum>(2)</enum><header>Small businesses</header><text>The Secretary shall, after consultation with the Small Business Administration and small businesses that manufacture cosmetics, provide additional guidance for small businesses on compliance with the requirements of this section. Such guidance shall include specific examples of options for compliance that do not place an undue burden on small businesses.</text></paragraph></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection commented="no" id="H463D1B99211D4BB8ACD8670FF495505C"><enum>(b)</enum><header>Effective date</header><text>Section 609 of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a), shall take effect 180 days after the date of enactment of this Act.</text>
</subsection><subsection id="H6C99F396F01849A19E23BCBD7337D1D2"><enum>(c)</enum><header>Public meeting and guidance</header>
<paragraph id="HE50C5D41369C4C3293DF6A7BBEF189F7"><enum>(1)</enum><header>Public meeting</header><text display-inline="yes-display-inline">Not later than 12 months after the date of the enactment of this Act, the Secretary of Health and Human Services (in this subsection referred to as the <quote>Secretary</quote>) shall convene a public meeting to describe and solicit public input regarding the ingredient review process under section 608 of the Federal Food, Drug, and Cosmetic Act (as added by subsection (a)). Such meeting shall include representatives from the cosmetics industry, medical practitioners and scientific experts with cosmetic expertise, and consumer and public health advocacy organizations.</text>
</paragraph><paragraph id="HA3ADDE9C36CB4380885B5492A001D541"><enum>(2)</enum><header>Guidance</header><text display-inline="yes-display-inline">Not less than one year after the public meeting conducted under paragraph (1), the Secretary shall issue one or more guidance documents to implement section 608 of the Federal Food, Drug, and Cosmetic Act (as added by subsection (a)). Such guidance documents shall include information regarding—</text>
<subparagraph id="HD6B4914984C04F6088415E9A275FB539"><enum>(A)</enum><text>the types of scientific evidence, clinical studies, data, or other information needed to support the review of cosmetic ingredients or nonfunctional constituents (or categories thereof) selected for review under such section;</text>
</subparagraph><subparagraph id="HF3A1D95FD484403EA965F15B6919CD18"><enum>(B)</enum><text>the recommended format in which to submit to the Secretary such data and information, including any applicable foreign data and information, related to a cosmetic ingredient or nonfunctional constituent (or category thereof) that has been selected for such review;</text>
</subparagraph><subparagraph id="H3DF1BEC89AF54CFE88EEFF6A30B8E973"><enum>(C)</enum><text>the manner and the number of days by which the Secretary intends to review and respond to such data and information, including with respect to providing a scientific rationale for any additional data and information;</text>
</subparagraph><subparagraph id="HB7EA92E9A3AD49FA815E58E75179A66E"><enum>(D)</enum><text>the process for communication between the Secretary and industry related to an ingredient or nonfunctional constituent (or a category thereof) that has been selected for review; and</text>
</subparagraph><subparagraph id="H222A9A74BC1B4587A67E16C4872A8C43"><enum>(E)</enum><text>includes such other information as the Secretary determines appropriate.</text> </subparagraph></paragraph><paragraph id="H20B7D1545F784ECB85D7B16F0DC270A7"><enum>(3)</enum><header>Timing</header><text display-inline="yes-display-inline">Not later than 24 months after the date of the enactment of this Act, the Secretary shall issue draft guidance under paragraph (1) on the implementation of section 608 of the Federal Food, Drug, and Cosmetic Act (as added by subsection (a)). The Secretary shall issue final guidance on the implementation of such section not later than 6 months after the date on which the comment period for the draft guidance closes.</text>
</paragraph></subsection><subsection id="HE0C74E48B1A3492EBB6514AD20DAA63D"><enum>(d)</enum><header>GAO study</header><text display-inline="yes-display-inline">Not later than 6 years after the date of the enactment of this Act, the Comptroller General of the United States shall submit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Health, Education, Labor, and Pensions of the Senate a report addressing the effectiveness and overall impact of the ingredient review program established under section 608 of the Federal Food, Drug, and Cosmetic Act (as added by subsection (a)), including with respect to its impact on the safety of cosmetic ingredients—</text>
<paragraph id="H0B1C1AD24D70442C931503C8BF305BA8"><enum>(1)</enum><text>for each ingredient or nonfunctional constituent (or category thereof) selected for review—</text> <subparagraph id="H98ECA4D5FA8841469454898D34F7A97D"><enum>(A)</enum><text>whether the ingredient or nonfunctional constituent (or category thereof) was determined—</text>
<clause id="HBCCE6CDC5A8746A6AB237FFCAB7B9FDD"><enum>(i)</enum><text>to be safe in cosmetic products without the need for specified conditions of use or tolerances;</text> </clause><clause id="H307CB9F05D8C471C828FE3E457E88091"><enum>(ii)</enum><text display-inline="yes-display-inline">to be safe in cosmetic products under specified conditions of use of tolerances; or</text>
</clause><clause id="H75C66A09A6B8492998D62DCD62EAADE7"><enum>(iii)</enum><text display-inline="yes-display-inline">to be not safe in cosmetic products;</text> </clause></subparagraph><subparagraph id="H8469E12AE3784ADC85D13E848FEB74D1"><enum>(B)</enum><text>the timeline for such review;</text>
</subparagraph><subparagraph id="HBA4CC7A2C06842E884F89E5DFDED45B0"><enum>(C)</enum><text>the types of scientific evidence, clinical studies, data, or other information used to make such a determination;</text>
</subparagraph><subparagraph id="H53C9DF7D379247F7B9910A94F5F40781"><enum>(D)</enum><text>whether, and to what extent, the review of the ingredient or nonfunctional constituent (or category thereof) resulted in cosmetic products being reformulated or removed from the market; and</text>
</subparagraph><subparagraph id="HD78D1D0A20684FBF89E2CD4E4016A591"><enum>(E)</enum><text>the impact the review and determination had on consumer use and access to such product; and</text> </subparagraph></paragraph><paragraph id="HE883DBEA7E964834971CA35E67E2AE03"><enum>(2)</enum><text>an analysis of the ingredient, nonfunctional constituent (or category thereof) review conducted under such section 608, including—</text>
<subparagraph id="H52D76BFA57FB40C1B38C90EFB197426C"><enum>(A)</enum><text>the resources used by the Secretary in reviewing ingredients and nonfunctional constituents (or categories thereof), including the effects of the program on other cosmetic safety activities of the Secretary;</text>
</subparagraph><subparagraph id="H26C16F2B61CA4FC0BC624783BAF1DAD8"><enum>(B)</enum><text>the impact of such section on innovation and consumer access to cosmetic products; and</text> </subparagraph><subparagraph id="HAE31C494A14C41DCA0C9BDCD72AB8D40"><enum>(C)</enum><text>whether any improvements to the program under such section 608 are necessary for increasing the efficiency and effectiveness of the review of cosmetic ingredients, nonfunctional constituents, or categories thereof.</text>
</subparagraph></paragraph></subsection></section><section commented="no" id="H0A089ECAB75C4BC584643C11A624FE47"><enum>103.</enum><header>Good manufacturing practices for cosmetics</header>
<subsection commented="no" id="H2726F89D43F1456D9FBB4BDE2C13F9BA"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 102, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="HBA0AC26FAFD24898A93E2F12FE426592" style="OLC">
<section id="H5A62267DC4694B708D339B60FDEAAA61"><enum>610.</enum><header>Good manufacturing practices for cosmetics</header>
<subsection id="H3F2D84757AD24FAD91B21E662BAC0714"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">The Secretary shall—</text> <paragraph id="HB315C61BA06C4AD28247C1EF6DE4FFA0"><enum>(1)</enum><text>review national and international standards for cosmetic good manufacturing practices that are in effect on the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>; and</text>
</paragraph><paragraph id="HBF05356510A74D2BB849F275386CC350"><enum>(2)</enum><text>issue a rule establishing current good manufacturing standards consistent, to the extent the Secretary determines practicable and appropriate, with such national and international standards.</text>
</paragraph></subsection><subsection id="H609711E95FED4B3D85BE06E6E8931582"><enum>(b)</enum><header>Content of regulations</header><text>The regulations issued pursuant to subsection (a)(2)—</text> <paragraph id="HEABC4B6ECBDE4BF9829BD1F0F1FEBAC7"><enum>(1)</enum><text display-inline="yes-display-inline">may specify requirements for the use of certain analytical or recordkeeping methods by a manufacturer as may be necessary to ensure that a cosmetic product or cosmetic formulation is not injurious to health under the recommended or suggested conditions of use, or customary or usual use of the product or formulation; and</text>
</paragraph><paragraph id="HA60639C0B346427BB6927DD1E2E1B6FA"><enum>(2)</enum><text>shall not—</text> <subparagraph id="H144A61FEC4864DB7A23550A90A0EF645"><enum>(A)</enum><text display-inline="yes-display-inline">impose standards for which there is no current and generally available analytic method; or</text>
</subparagraph><subparagraph id="H4B49B7ED7C234BE88A5D9192D7207C1D"><enum>(B)</enum><text>apply to facilities meeting the criteria to be considered a facility under section 604(6), including retail stores or counters offering customized or personalized cosmetics to consumers, or to entities that are in compliance with the good manufacturing practice regulations specified in parts 210 and 211 of title 21, Code of Federal Regulations (or any successor regulations). <italic></italic></text>
</subparagraph></paragraph></subsection><subsection id="HE7E23B9CC040461F8104EB1E6D9906EE"><enum>(c)</enum><header>Timeframe</header><text display-inline="yes-display-inline">The Secretary shall publish a proposed rule described in subsection (a) not later than 24 months after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title> and shall publish a final such rule not later than 36 months after such date of enactment.</text></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection id="H7143E09E97EC46A1AAD185F917956C22"><enum>(b)</enum><header>Effective date for cosmetic manufacturers</header><text display-inline="yes-display-inline">Regulations issued pursuant to section 610 of the Federal Food, Drug, and Cosmetic Act (as added by subsection (a)) shall apply with respect to—</text>
<paragraph id="H4758AEE2CB14481D9B3900209A90DF79"><enum>(1)</enum><text>large manufacturers (as defined in section 744L of such Act (as added by section 202 of this Act)), beginning 180 days after the date on which the final rule described in subsection (a) is effective;</text>
</paragraph><paragraph id="H0CC5A296198E4A279DCB2462250918BA"><enum>(2)</enum><text display-inline="yes-display-inline">midsize manufacturers (as defined in section 744L of such Act (as added by section 202 of this Act)), beginning 210 days after such date; and</text>
</paragraph><paragraph id="H0378272663FB4A3D95C49707868D2222"><enum>(3)</enum><text display-inline="yes-display-inline">small manufacturers (as defined in section 744L of such Act (as added by section 202 of this Act)), beginning 2 years after such date.</text>
</paragraph></subsection><subsection commented="no" id="H619EFD12AE1F4658B1DA6DF27F0B9AC7"><enum>(c)</enum><header>Enforcement</header><text display-inline="yes-display-inline">Section 601 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref>) is amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H16D497D3FABA47F5BC1AE831D6C9A648" style="OLC">
<subsection commented="no" id="H4C3BB737984A40988CBA6B0AEA35EE17"><enum>(f)</enum><text>If the methods used in, or the facilities or controls used for, its manufacture, processing, packing, or holding do not conform to current good manufacturing practice, as prescribed by the Secretary.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection></section><section commented="no" id="H7A8DC913415745998C876DA2F2C9BBDB"><enum>104.</enum><header>Adverse event reports</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 103(a), is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="HB4102E20518D49688D7C87E25BE8539A" style="OLC">
<section commented="no" id="H2430926909694CAC9D95138F38516214"><enum>611.</enum><header>Adverse event reporting for cosmetics</header>
<subsection commented="no" id="H220FF752A965427F8D346310E05FF5B0"><enum>(a)</enum><header>Submission of serious adverse event reports</header>
<paragraph id="HAE774F36BE7B4A71AC4B28F8C74174C9"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">With respect to any cosmetic product distributed in the United States, the responsible person shall submit, not later than 15 days after the receipt by the responsible person, using an electronic system developed under subsection (b), to the Secretary any report of a serious adverse event associated with the use of the cosmetic product, accompanied by a copy of the label on or with the retail packaging of the cosmetic product.</text>
</paragraph><paragraph id="H136B972091A740FB97A0ED01D48776BF"><enum>(2)</enum><header>New medical information</header><text display-inline="yes-display-inline">During the 12-month period following the submission of a serious adverse event report under paragraph (1), with respect to any cosmetic product distributed in the United States, the responsible person shall submit, not later than 15 days after the receipt by the responsible person, using an electronic system developed under subsection (b), to the Secretary any new medical information related to such serious adverse event report that is received by the responsible person<italic>.</italic></text>
</paragraph><paragraph id="H5808DC8829754CAAAE1307E6F503FCC8"><enum>(3)</enum><header>Publication</header><text display-inline="yes-display-inline">The Secretary shall make publicly available on the internet website of the Food and Drug Administration reports submitted under paragraph (1).</text>
</paragraph><paragraph commented="no" id="H7254F6502CFD4A689BD2878AF9DF99C2"><enum>(4)</enum><header>No duplication</header><text display-inline="yes-display-inline">In the case of cosmetic product that is also a drug for which a serious adverse event report is filed using Form FDA 3500A (or any successor form developed for such purpose) or its electronic equivalent for over-the-counter drugs, the responsible person shall not be required to submit a serious adverse event report under paragraph (1) with respect to that cosmetic product.</text>
</paragraph></subsection><subsection commented="no" id="H03C01DC71EC8413B9CEFAAF9568AF178"><enum>(b)</enum><header>Requirements for serious adverse event reports</header>
<paragraph commented="no" id="H4D9AA566170C453180A78DC5CD938517"><enum>(1)</enum><header>Electronic system</header>
<subparagraph id="HAC16F745C6CE4144B39810EF27818EE8"><enum>(A)</enum><header>In general</header><text>The Secretary shall, not later than 1 year after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, develop and implement an electronic system for use for the submission of serious adverse event reports under this section.</text>
</subparagraph><subparagraph commented="no" id="HABE9652975C34BF0A30894EF0AE5F58D"><enum>(B)</enum><header>Modification</header><text>The format of the electronic system developed and implemented under paragraph (1) may be modified by the Secretary and the reports may include additional information. The Secretary may, in guidance, further specify the format and contents of required reports.</text>
</subparagraph></paragraph><paragraph commented="no" id="H9CD62EE28FD741948CF7CDC3B1C8F037"><enum>(2)</enum><header>Content of reports</header><text>A serious adverse event report submitted under paragraph (1) of subsection (a) shall include all information submitted with the initial report and any information subsequently added to such report pursuant to paragraph (2) of such subsection and—</text>
<subparagraph commented="no" id="H77FC35E23EF8409F95C424E8D8ABE84D"><enum>(A)</enum><text>any report by the responsible person under section 756 with respect to the safety of the cosmetic product that is the subject of the report;</text>
</subparagraph><subparagraph commented="no" id="H1D76C46D814D464DA910DE4637B30CAF"><enum>(B)</enum><text>information on the individual or individuals with respect to whom the adverse event report is submitted, in accordance with the disclosure requirements of section 552a of title 5, United States Code;</text>
</subparagraph><subparagraph commented="no" id="H9386751C53C54D6CB414C55EF6F19CBB"><enum>(C)</enum><text display-inline="yes-display-inline">notwithstanding section 552(b)(6) of title 5, United States Code, medical (or similar) documentation of the serious adverse event that is the subject of the report, with all personally identifiable information redacted; and</text>
</subparagraph><subparagraph commented="no" id="H6427FAAEF58E4AFC926D7FD4F8441CA5"><enum>(D)</enum><text>contact information for the individual or individuals reporting the serious adverse event.</text> </subparagraph></paragraph><paragraph commented="no" id="H7C01A5EB567C4BB6B93AAE53BB0777B9"><enum>(3)</enum><header>Responsibility to gather information</header><text>After an individual initiates the reporting of a serious adverse event, the responsible person for the cosmetic product shall actively gather all of the information reasonably available to such person to complete and file the report with the Secretary under subsection (a)(1).</text>
</paragraph><paragraph commented="no" id="H92EDBE8A57D6485686DAF6BC8F1EE8C7"><enum>(4)</enum><header>No adverse events to report</header><text><italic></italic>The Secretary shall provide an option as part of the electronic registration process for the responsible person to indicate if such responsible person had no adverse events to report over the previous year. With respect to a responsible person who received no adverse event reports for a year, the annual adverse event report requirement may be met by indicating no such events on the annual registration form.</text>
</paragraph><paragraph commented="no" id="H2050155EDA254A11BA7C5FF1AB0805D2"><enum>(5)</enum><header>Exemption</header><text>The Secretary may establish by regulation an exemption to any of the requirements under this section if the Secretary determines that such exemption is supported by adequate evidence and would have no adverse effect on public health.</text>
</paragraph></subsection><subsection commented="no" id="HA1635A9F3EC7425EAF646352FB3947C3"><enum>(c)</enum><header>Requirements for other adverse event reports</header>
<paragraph commented="no" id="H84DF472872934C4D97597AE626649E0A"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">Each responsible person shall maintain records related to each report of an adverse event (including serious adverse events) associated with each cosmetic product marketed by such responsible person and received by such responsible person for a period of 6 years. Such records shall be made available to an officer or an employee duly designated by the Secretary upon request, at reasonable times and within reasonable limits and in a reasonable manner, including allowing electronic access and to copy such records.</text>
</paragraph><paragraph commented="no" id="H934255D0EE1F452284B4DDFD07F5085A"><enum>(2)</enum><header>Content</header><text display-inline="yes-display-inline">Records required to be maintained under this paragraph shall contain all information reasonably available, including—</text>
<subparagraph commented="no" id="H4D63631D224045B29C7C27D2B8456D29"><enum>(A)</enum><text display-inline="yes-display-inline">a summary of all adverse events received during the calendar year for each cosmetic product marketed;</text>
</subparagraph><subparagraph commented="no" id="HBF3E039C077847F9BA469E7257F1F426"><enum>(B)</enum><text display-inline="yes-display-inline">a complete list of individual reports of adverse events for each cosmetic product marketed and with respect to each such event, the same information required to be included in a report with respect to a serious adverse event under subsection (b)(2), subject to the same conditions with respect to the disclosure of such information;</text>
</subparagraph><subparagraph id="HD6180B949C5A427D8352A3C346109490"><enum>(C)</enum><text>an estimate of the total number of product units estimated to have been distributed to consumers during the period specified in paragraph (1); and</text>
</subparagraph><subparagraph id="HCF334FF26E2948D29EEF9CB8871F1BF8"><enum>(D)</enum><text>such other information as may be specified in regulation or guidance issued by the Secretary.</text> </subparagraph></paragraph><paragraph id="HA6E629C050504E639430C2047CCE91B7"><enum>(3)</enum><header>Rule of construction</header><text display-inline="yes-display-inline">This section shall not be construed to require the inclusion in any report under this section any consumer complaint that concerns solely efficacy and does not contain any information about an adverse event.<italic></italic><italic></italic></text>
</paragraph></subsection><subsection commented="no" id="H47E0F40686C943C4A0BC690A17403419"><enum>(d)</enum><header>Limitation with respect to adverse event reports</header><text display-inline="yes-display-inline"><italic></italic> Section 756 shall apply with respect to the submission of an adverse event report in compliance with subsection (a).</text>
</subsection><subsection commented="no" id="HE7C1B032F6A74FD3AE10FCE2930903D9"><enum>(e)</enum><header>Contact information</header><text display-inline="yes-display-inline">The label of a cosmetic product shall bear the domestic address, and either the domestic telephone number or electronic contact information, through which the responsible person may receive a report of an adverse event.</text>
</subsection><subsection commented="no" id="HE168DEC6BF074C27BAFEA669E722FAE2"><enum>(f)</enum><header>Availability to States</header><text display-inline="yes-display-inline">The Secretary shall make records submitted under this section available to any State, upon request, to the extent permissible under the laws governing disclosure of information by the Secretary. Information disclosed to a State that is exempt from disclosure under section 552(b)(4) of title 5, United States Code, shall be treated as a trade secret and confidential information by the State. Such State and its employees in possession of such information shall be subject to the same laws governing information disclosure as employees of the Food and Drug Administration.</text>
</subsection><subsection commented="no" id="H4DA03331FCC54896A3DBE009888AF8A2"><enum>(g)</enum><header>Protection of information</header><text display-inline="yes-display-inline">A serious adverse event report submitted to the Secretary under subsection (a), including any new medical information submitted under paragraph (2) of such subsection, or an adverse event report voluntarily submitted to the Secretary, shall be considered to be a safety report under section 756 and may be accompanied by a statement, which shall be a part of any report that is released for public disclosure, that denies that the report or the records constitute an admission that the product involved caused or contributed to the adverse event.</text>
</subsection><subsection commented="no" id="H43D6A329BB4E4A6C93549CEB4F82C1FB"><enum>(h)</enum><header>Effective dates</header>
<paragraph commented="no" id="H29D80EE6D04949A0BF07E871A9EA13F7"><enum>(1)</enum><header>Serious adverse events</header><text display-inline="yes-display-inline">The requirement under this section to report serious adverse events shall become effective on the date that the Secretary publicizes the availability of the electronic system described in subsection (b)(1).</text>
</paragraph><paragraph commented="no" id="H173A604EF61140DC9BB15C0433F5AEDB"><enum>(2)</enum><header>Other adverse events</header><text display-inline="yes-display-inline">The requirement under this section to maintain records relating to adverse events which are not serious adverse events shall become effective 18 months after the date of the enactment of the Cosmetic Safety Enhancement Act of 2019.</text>
</paragraph></subsection><subsection commented="no" id="HDA28470D929442C4B3D029426FB876CB"><enum>(i)</enum><header>Definitions</header><text>In this section:</text> <paragraph commented="no" id="H37D6D1E68CCD4B3698852193F533E921"><enum>(1)</enum><header>Adverse event</header><text display-inline="yes-display-inline">The term <term>adverse event</term> means, with respect to a cosmetic product, a health-related or medical event associated with the use of such product, including a risk of illness or injury. Such term does not include any instance of a consumer complaint that such product did not work as advertised or marketed.</text>
</paragraph><paragraph commented="no" id="H4CB437987F5348E4B9FECF4A81FE97F7"><enum>(2)</enum><header>Serious adverse event</header><text>The term <term>serious adverse event</term> means, with respect to a cosmetic product, an adverse event that—</text> <subparagraph commented="no" id="H22F2DBDFE03747D283F31DDFA354E02C"><enum>(A)</enum><text>results in—</text>
<clause commented="no" id="HD8A0E252644541FF8D1CD387844D744E"><enum>(i)</enum><text>death;</text> </clause><clause commented="no" id="H17AB27EC52D74FAC8ECC0C16655F3807"><enum>(ii)</enum><text>a life-threatening experience;</text>
</clause><clause commented="no" id="HA5550FE197BD4309BFF06E944ECF6E39"><enum>(iii)</enum><text>inpatient hospitalization;</text> </clause><clause commented="no" id="H0D22751DFA03464EAB7B312C273220B2"><enum>(iv)</enum><text>a persistent or significant adverse health condition, disability, or incapacity;</text>
</clause><clause commented="no" id="HF8BDBBA7A1994EEE873C67DE147420F7"><enum>(v)</enum><text>congenital anomaly or birth defect; or</text> </clause><clause commented="no" id="HA5EF0AA3422441DEB75343242465DC2C"><enum>(vi)</enum><text>significant disfigurement, including serious or persistent rashes and infections, burns, or significant hair loss; or</text>
</clause></subparagraph><subparagraph commented="no" id="HC04198FF4B9E4D3BB04FC1830AC69358"><enum>(B)</enum><text>requires, based on reasonable medical judgment, a medical or surgical intervention to prevent an outcome described in subparagraph (A).</text></subparagraph></paragraph></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section commented="no" id="HA86D0AE22F924F71B78D6D63F611FC9D"><enum>105.</enum><header>Records inspection; mandatory recall authority</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 104, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H2694D640496149B6A3BB64B730BDA2C2" style="OLC">
<section commented="no" id="HEFBBA413F338448BB6799E1D5A990428"><enum>612.</enum><header>Inspection of cosmetic records</header>
<subsection commented="no" id="HED2EBE221D1E48FEA02AB9CC27F1D7C6"><enum>(a)</enum><header>Inspection of records</header><text display-inline="yes-display-inline">Each facility, including a facility owned or operated by a responsible person for a cosmetic product shall, at the request of an officer or employee duly designated by the Secretary, permit such officer or employee, upon presentation of appropriate credentials and written notice to such person, at reasonable times and within reasonable limits and in a reasonable manner, to have access to and copy, or receive electronically records maintained by or on behalf of such person in any format (including paper and electronic formats) and at any location, including—</text>
<paragraph commented="no" id="H602D78D360784DF39FA327A687CA6198"><enum>(1)</enum><text>all records maintained under section 611 and in accordance with the rules promulgated by the Secretary under section 610, as applicable;</text>
</paragraph><paragraph commented="no" id="H46D5A61C06C14DB9903018AA5FF226BE"><enum>(2)</enum><text display-inline="yes-display-inline">all records maintained under section 609;</text> </paragraph><paragraph id="HDF3C494FAA264E398BC2F812D873F9C0"><enum>(3)</enum><text display-inline="yes-display-inline">any records relating to the list of ingredients in specific fragrances or flavors of a cosmetic product or cosmetic formulation, if requested by the Secretary by means of a written notification; and</text>
</paragraph><paragraph commented="no" id="HEA25CA2A813F465ABAA64C10B11040CA"><enum>(4)</enum><text display-inline="yes-display-inline">except as provided in subsection (b), all other records relating to the cosmetic product or cosmetic formulation and to any other cosmetic product or cosmetic formulation the Secretary reasonably believes is likely to be affected in a similar manner, if the Secretary—</text>
<subparagraph commented="no" id="HC86676C427AE4E6BB18385989F6CD56D"><enum>(A)</enum><text>has a reasonable belief that the cosmetic product or cosmetic formulation—</text> <clause commented="no" id="HBBF8AD088B3042C4A6E72914B4FB7DA7"><enum>(i)</enum><text>is adulterated;</text>
</clause><clause commented="no" id="HD05994C3381040009E7E327AAAE8A635"><enum>(ii)</enum><text>has caused a reportable serious adverse event; or</text> </clause><clause commented="no" id="HF09903D7E8D84F6D99C2F01BAB914CCE"><enum>(iii)</enum><text>contains an ingredient for which new scientific information shows may be unsafe when present in a cosmetic product or cosmetic formulation; and</text>
</clause></subparagraph><subparagraph commented="no" id="H1667E3385FD84A0FA1EB98A1EC824148"><enum>(B)</enum><text display-inline="yes-display-inline">provides written notice to the responsible person of the basis for the Secretary’s reasonable belief described in subparagraph (A), as applicable.</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="H69DC87D1C4C947DB811532A82BECC631"><enum>(b)</enum><header>Exclusions</header>
<paragraph id="H605CE3AA0F2948ABA0EEDDFD33F6FE7C"><enum>(1)</enum><header>In general</header><text>No inspection authorized by this section shall extend to—</text> <subparagraph id="H22192975AB2A4195A6E3D978B3643FD0"><enum>(A)</enum><text>recipes, financial data, pricing data, personnel data (other than data as to qualification of technical and professional personnel performing functions subject to this Act), research data (other than safety data) or sales data other than shipment and distribution data; or</text>
</subparagraph><subparagraph id="HD6024027DA924CF1A2BFEBC7F143A982"><enum>(B)</enum><text display-inline="yes-display-inline">except as provided in paragraph (2), information related to ingredients in fragrances or flavors of a cosmetic product or cosmetic formulation.</text>
</subparagraph></paragraph><paragraph id="H1F5E5AEBF3884DF5B2427DB2B87B8D4F"><enum>(2)</enum><header>Exception</header><text display-inline="yes-display-inline">The Secretary may obtain information related to the ingredients in fragrances or flavors in an identified cosmetic product or cosmetic formulation only by a request in a written notification provided to the manufacturer pursuant to a for-cause inspection. In response to such written notification, the manufacturer of such fragrance or flavor shall provide information about the ingredients in the specified fragrance or flavor that the Secretary determines is necessary to assist its investigation, in the manufacturer’s preferred electronic or written format, to the Secretary upon receipt of such notification. Any information provided in response to such written notification shall be considered a trade secret under section 301(j) and, notwithstanding such section, shall only be disclosed if the Secretary determines such disclosure is necessary to protect the public health. The authority to determine such disclosure is necessary to protect the public health shall not be delegated to any officer or employee other than the director of the applicable office.</text>
</paragraph></subsection><subsection commented="no" id="H04738460FE2C4D9F909F93075A6B6D6F"><enum>(c)</enum><header>Protection of sensitive information</header><text display-inline="yes-display-inline">The Secretary shall take appropriate measures to ensure that there are effective procedures to prevent the unauthorized disclosure of any trade secret or confidential information that is obtained by the Secretary pursuant to this section. Information disclosed to a State shall be pursuant to the laws governing disclosure of information. Confidential information disclosed to the State that is exempt from disclosure under section 552(b)(4) of title 5, United States Code, shall be treated as confidential information by the State. Such State and its employees in possession of such information under this section shall be subject to the same laws governing information disclosure as employees of the Food and Drug Administration.</text>
</subsection><subsection commented="no" id="H949F61A5C40D4F1781FEA8B151DD7CDF"><enum>(d)</enum><header>Limitations</header><text>This section shall not be construed—</text> <paragraph commented="no" id="H4849AEFF7C60432D8AC9B5E9EC1BB42C"><enum>(1)</enum><text>to limit the authority of the Secretary to inspect records or to require establishment and maintenance of records under any other provision of this Act; or</text>
</paragraph><paragraph commented="no" id="H253D774D42C74254B7598A8327E8B3C8"><enum>(2)</enum><text display-inline="yes-display-inline">to require the Secretary to publicly disclose any information that is exempt from disclosure under section 522 of title 5, United States Code, or section 1905 of title 18, United States Code.</text>
</paragraph></subsection></section><section commented="no" id="HFF02E2B134B444709C8BBFCDE0E57D6A"><enum>613.</enum><header>Mandatory recall authority</header>
<subsection commented="no" id="HCD04598374C449C4B74026D9AE9A75BA"><enum>(a)</enum><header>Voluntary procedures</header><text>If the Secretary determines that there is a reasonable probability that a cosmetic product is adulterated under section 601 or misbranded under section 602 and the use of, and exposure to, such cosmetic product is likely to cause serious adverse health consequences or death, the Secretary shall provide the responsible person with an opportunity to voluntarily cease distribution and recall such article.</text>
</subsection><subsection commented="no" id="H09F78358568F4CD2A7982639C81C9E88"><enum>(b)</enum><header>Prehearing order To mandatorily cease distribution and give notice</header>
<paragraph commented="no" id="H5C4C1CD97EBE443097EBE9B8074890C2"><enum>(1)</enum><header>In general</header><text>If the domestic responsible person refuses to or does not voluntarily cease distribution or recall such cosmetic product within the time and in the manner prescribed by the Secretary, the Secretary may order such person to—</text>
<subparagraph commented="no" id="H83CEAB6CE3AF4B5EBDF43D3379E48694"><enum>(A)</enum><text>immediately cease distribution of such cosmetic product; and</text> </subparagraph><subparagraph commented="no" id="H896C2058D8E14A50BDCCA193DDDE1D3A"><enum>(B)</enum><text>as applicable, immediately order all facilities—</text>
<clause commented="no" id="H8364817615534B01A26C1F84857BCDA5"><enum>(i)</enum><text>manufacturing, processing, packing, transporting, holding, receiving, distributing, or importing and selling such cosmetic product; and</text>
</clause><clause commented="no" id="H34F87B3009E244EB8AA34235F4930C77"><enum>(ii)</enum><text>to which such cosmetic product has been distributed, transported, or sold,</text> </clause><continuation-text commented="no" continuation-text-level="subparagraph">to immediately cease distribution of such cosmetic product.</continuation-text></subparagraph></paragraph><paragraph commented="no" id="H1049E63906CC40DCAF0F15A0DDB447F7"><enum>(2)</enum><header>Required additional information</header> <subparagraph commented="no" id="H28E22818673D47A19128E9FBA7D8583A"><enum>(A)</enum><header>In general</header><text>In the case of a cosmetic product that is subject to a recall order issued under paragraph (1)(B) with respect to which the responsible person, before the issuance of such order, distributed to a warehouse-based, third-party logistics provider without providing such logistics provider with sufficient information to know or reasonably determine the precise identity of such cosmetic product, the notice provided by the domestic responsible person pursuant to such order shall include such information as is necessary for the logistics provider to identify the cosmetic product.</text>
</subparagraph><subparagraph commented="no" id="H523BF2CD009F49F19305B920E84F65A9"><enum>(B)</enum><header>Rules of construction</header><text display-inline="yes-display-inline">Nothing in this paragraph shall be construed to exempt a warehouse-based, third-party logistics provider from—</text>
<clause commented="no" id="H8C7A04AF5CC1425C992FF96862892CD9"><enum>(i)</enum><text>the requirements of this chapter, including the requirements of this section and section 612; or</text> </clause><clause commented="no" id="HB43D94DD76234BA6BFE14A51B8C6F146"><enum>(ii)</enum><text>being the subject of a mandatory recall order under this section.</text>
</clause></subparagraph></paragraph><paragraph commented="no" id="HF1C369428D78416DB6B90AB4F942C126"><enum>(3)</enum><header>Determination to limit areas affected</header><text>If the Secretary requires a domestic responsible person to cease distribution under paragraph (1)(A) of a cosmetic product, the Secretary may limit the size of the geographic area and the markets affected by such cessation if such limitation would not compromise the public health.</text>
</paragraph></subsection><subsection commented="no" id="H4ABC81A08C8E48B0873A21D9E2B6915C"><enum>(c)</enum><header>Hearing on order</header><text>The Secretary shall provide the responsible person subject to an order under subsection (b) with an opportunity for an informal hearing, to be held as soon as possible, but not later than 2 days after the issuance of the order, on the actions required by the order and on why the cosmetic product that is the subject of the order should not be recalled.</text>
</subsection><subsection commented="no" id="H55B38E18DF6446FEA1CB7A7A04265D0A"><enum>(d)</enum><header>Posthearing recall order and modification of order</header>
<paragraph commented="no" id="HF96D4DCDAFA34D1B9C9E1AC7262F99B7"><enum>(1)</enum><header>Amendment of order</header><text>If, after providing opportunity for an informal hearing under subsection (c), the Secretary determines that removal of the cosmetic product from commerce is necessary, the Secretary shall, as appropriate—</text>
<subparagraph commented="no" id="H645F7D209FD94C09A34FC82A3B5705FE"><enum>(A)</enum><text>amend the order to require recall of such cosmetic product or other appropriate action;</text> </subparagraph><subparagraph commented="no" id="HCBF129333D5945198F627CD416DF5428"><enum>(B)</enum><text>specify a timetable in which the recall shall occur;</text>
</subparagraph><subparagraph commented="no" id="HC2B286791E68421D837D56D0048AC0BC"><enum>(C)</enum><text>require periodic reports to the Secretary describing the progress of the recall; and</text> </subparagraph><subparagraph commented="no" id="H6C011ED39CAB48F1851784D6EAD37AE1"><enum>(D)</enum><text>provide notice to consumers to whom such cosmetic product was, or may have been, distributed.</text>
</subparagraph></paragraph><paragraph commented="no" id="HC900C44199A54067AB0FD5478F97E482"><enum>(2)</enum><header>Vacating of order</header><text>If, after such hearing, the Secretary determines that adequate grounds do not exist to continue the actions required by the order, or that such actions should be modified, the Secretary shall vacate the order or modify the order.</text>
</paragraph></subsection><subsection commented="no" id="H2BDB3E120F1146D0848001A371DC8F44"><enum>(e)</enum><header>Cooperation and consultation</header><text>The Secretary shall work with State and local public health officials in carrying out this section, as appropriate.</text>
</subsection><subsection commented="no" id="H31B408416489469389E4F268B846F101"><enum>(f)</enum><header>Public notification</header><text>In conducting a recall under this section, the Secretary shall—</text> <paragraph commented="no" id="HE6B482CE8DEB47F8B016D5D50A2D20C1"><enum>(1)</enum><text>ensure that a press release is published regarding the recall, and that alerts and public notices are issued, as appropriate, in order to provide notification—</text>
<subparagraph commented="no" id="H10193E57FFF043AF8F2BF35111BF1A1B"><enum>(A)</enum><text>of the recall to consumers and retailers to whom such cosmetic product was, or may have been, distributed; and</text>
</subparagraph><subparagraph commented="no" id="HCFA0198FBA714EC1A099D3538BB3683D"><enum>(B)</enum><text>that includes, at a minimum—</text> <clause commented="no" id="H3FE631B85CC44BAE88B51BE7C7A425C9"><enum>(i)</enum><text>the name of the cosmetic product subject to the recall;</text>
</clause><clause commented="no" id="H4A9194CFFA9A4B2C87B798CD5FAB4274"><enum>(ii)</enum><text>a description of the risk associated with the use of such cosmetic product; and</text> </clause><clause commented="no" id="H7C17C6E804274644954E52355FA4EEFD"><enum>(iii)</enum><text>to the extent practicable, information for consumers about similar cosmetic products that are not affected by the recall; and</text>
</clause></subparagraph></paragraph><paragraph commented="no" id="HF74E55AB047146C2A5CE779E9097598B"><enum>(2)</enum><text>ensure publication on the internet website of the Food and Drug Administration of an image of the cosmetic product that is the subject of the press release described in paragraph (1), if available.</text>
</paragraph></subsection><subsection commented="no" id="H653592E0E3ED44F5B3C858E6BB86F783"><enum>(g)</enum><header>No delegation</header><text>The authority conferred by this section to order a recall or vacate a recall order shall not be delegated to any officer or employee other than the Commissioner of Food and Drugs.</text>
</subsection><subsection commented="no" id="HD6EF93FC69264855A87A364A15768DFE"><enum>(h)</enum><header>Rule of construction</header><text>Nothing in this section shall affect the authority of the Secretary to request or participate in a voluntary recall, or to issue an order to cease distribution or to recall any article under any other provision of this Act or under the Public Health Service Act.</text>
</subsection><subsection id="H223B6622AE1F4B0191086ECD5FDFE4C8"><enum>(i)</enum><header>Definition</header><text>In this section, the term <term>domestic responsible person</term> means a person who is the domestic contact for a responsible person.</text></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block> </section><section id="HF7A5032AB70D4A6082920D3A5F8D3733"><enum>106.</enum><header>Labeling and internet sales</header> <subsection id="H3C0B677B917A47829B214F6E5D14F249"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 105, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H1E3D8BFF77D64269A7463B300C5271C0" style="OLC">
<section id="HF7471B7F21134DF8A4C2E86CA1442E5E"><enum>614.</enum><header>Labeling and internet sales</header>
<subsection id="H0E644989AB8248ADA579EE76A9457883"><enum>(a)</enum><header>Safety review and labeling</header><text>If a warning or condition of use is required pursuant to section 608(d)(4) to ensure the safe use of a cosmetic ingredient, the Secretary shall require appropriate labeling of any cosmetic product that contains such ingredient, including if such ingredient—</text>
<paragraph id="HDF78319558364AADB47180A7E7007D77"><enum>(1)</enum><text>is not appropriate for use in the entire population; or</text> </paragraph><paragraph id="H291755E4B4894382A34E57A088BDFEA2"><enum>(2)</enum><text>requires warnings that children, pregnant women, and other vulnerable populations should limit or avoid using the product.</text>
</paragraph></subsection><subsection id="HE7F3FE13DB7642B88F0F9A6661D3365F"><enum>(b)</enum><header>Cosmetic products for professional use</header>
<paragraph id="HCDCC2063BCEF46589D1E521741248EF5"><enum>(1)</enum><header>Listing of ingredients</header><text>The labeling of cosmetic products used and sold by professionals shall list all ingredients, as required for other cosmetic products pursuant to section 602(g).</text>
</paragraph><paragraph id="H4921539D50A540A9A5815B0B7116DB4F"><enum>(2)</enum><header>Professional use labeling</header><text>In the case of a cosmetic product that is intended to be used only by a professional on account of a specific ingredient or increased concentration of an ingredient and requires safe handling by trained professionals, the product shall bear a statement as follows: <quote>For Professional Use Only</quote>.</text>
</paragraph></subsection><subsection id="HA75DB3D85E6140FCB2C628952A64E085"><enum>(c)</enum><header>Display</header><text>A warning required under subsection (a) and any statement required under subsection (b)(2) shall be prominently displayed—</text>
<paragraph id="H359421F4FDB14CFE9B68F64E4959DC88"><enum>(1)</enum><text>in the primary language used on the label or on packaging; and</text> </paragraph><paragraph id="HB3B086F0A1DA449CB10237AE83992650"><enum>(2)</enum><text>in conspicuous and legible type in contrast by typography, layout, or color with other material printed or displayed on the label.</text>
</paragraph></subsection><subsection id="H98B24B79448548DD9C796070E12A9A6A"><enum>(d)</enum><header>Internet sales</header>
<paragraph id="H868C6B8503B74C32A75376A5B6502667"><enum>(1)</enum><header>In general</header><text>In the case of internet sales of cosmetic products, each primary seller offering a cosmetic product for sale to consumers on an internet website shall prominently and conspicuously display on such internet website—</text>
<subparagraph id="H7BB0420D431448C7BCB31DBBDC193CEB"><enum>(A)</enum><text>the same information that is included on the packaging of the cosmetic product as regularly available, such as any warnings, ingredient list, and contact information; and</text>
</subparagraph><subparagraph id="H8FC5B51FE1D849B8A02E9B67D4292707"><enum>(B)</enum><text>the warnings and statements described in subsection (c).</text> </subparagraph></paragraph><paragraph id="HA79E696D3FC4424F9290E36F37B0D0C0"><enum>(2)</enum><header>Definition</header><text display-inline="yes-display-inline">For purposes of this subsection, the term <term>primary seller</term> refers to the entity who offers a cosmetic product for sale on an internet website, including the responsible person.</text>
</paragraph></subsection></section><section id="H2B48ABE7C7604651B778C2911B8132B6"><enum>615.</enum><header>Fragrance ingredients</header>
<subsection id="HF3D0BAF4DA0747C6B4C68FE8276CBA95"><enum>(a)</enum><header>Fragrance ingredients</header><text display-inline="yes-display-inline">Not later than 2 years after the date of enactment of the Cosmetic Safety Enhancement Act of 2019, the responsible person shall include on the label of any cosmetic products containing one or more fragrance allergens, a list of each such fragrance allergen included in such cosmetic product that is consistent with national and international regulations for fragrance allergens labeling.</text>
</subsection><subsection id="HBCC2FC2173C04B04945E13AC4CF14D0A"><enum>(b)</enum><header>Contact information</header>
<paragraph id="HF971E62F7A244D8EB06B24BFECBF40E0"><enum>(1)</enum><header>In general</header><text>The contact information on the label on a cosmetic product for consumers to report adverse events shall also provide a means for consumers to obtain additional information about the inclusion of any recognized fragrance allergen required to be included on such label under subsection (a).</text>
</paragraph><paragraph id="H9B323C8F59DA4B9DBD5DA0839EA0A822"><enum>(2)</enum><header>Response</header>
<subparagraph id="HBA3DC757E50D42A08F0CBEB925591A4E"><enum>(A)</enum><header>In general</header><text>The responsible person shall—</text> <clause id="H245A63E6E8344F7B880E725243A113D7"><enum>(i)</enum><text display-inline="yes-display-inline">upon receipt of a request for information under paragraph (1), promptly obtain and provide such information to the requesting consumer; and</text>
</clause><clause id="H3E481193CD184AFFAB656FD437350CFC"><enum>(ii)</enum><text>in the case of information in the possession of a supplier, promptly obtain such information from such supplier, if reasonably available.</text>
</clause></subparagraph><subparagraph id="H1BE354857B8D4747A308370ABB016A76"><enum>(B)</enum><header>Supplier</header><text>A supplier shall promptly provide information requested pursuant to subparagraph (A)(ii).</text></subparagraph></paragraph></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block> </subsection><subsection id="H8D936C5C43194824ABFC59E8B7EF9C3F"><enum>(b)</enum><header>Ingredient statement</header><text>Section 602 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/362">21 U.S.C. 362</external-xref>) is amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H347C6D68EAD143FEACBA658223CCCB2C" style="OLC">
<subsection id="H73FD6DB320D64E3AB8FF90C0C47BB7C5"><enum>(g)</enum><text display-inline="yes-display-inline">If its labeling or packaging does not contain a listing of ingredients that meets the requirements of part 701 of title 21, Code of Federal Regulations (as in effect on date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>) (or any successor regulations).</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection id="H34A8AF60E395446EAF8AE9A5438F64E6"><enum>(c)</enum><header>Effective date</header><text display-inline="yes-display-inline">The amendments made by this section shall apply with respect to products introduced or delivered for introduction into interstate commerce on or after the date that is 2 years after the date of enactment of this Act.</text>
</subsection></section><section id="H69F0E34725AC4307881164760007810D"><enum>107.</enum><header>Consumer information</header><text display-inline="no-display-inline">The Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall post on its internet website information for consumers regarding—</text>
<paragraph id="H017D536652984551B35F7B71DAE274E9"><enum>(1)</enum><text display-inline="yes-display-inline">final orders regarding the safety of a cosmetic ingredient or nonfunctional constituent under section 608(d)(3);</text>
</paragraph><paragraph id="HF99BAE350EE342D7998C023D3F183036"><enum>(2)</enum><text>cosmetic product recalls (including voluntary and mandatory recalls); and</text> </paragraph><paragraph id="H8EA0287B861A4756BB61A822D72152DD"><enum>(3)</enum><text>identified counterfeit cosmetic products.</text>
</paragraph></section><section id="H89323CB9435848319A2FAC765C9E77BB"><enum>108.</enum><header>Small businesses</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 106, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H11A320B1BE1342B78D1D7DDAA5E77F54" style="OLC">
<section id="H17693176AB1D484CBE267B4FFC709BB5"><enum>616.</enum><header>Small businesses</header>
<subsection id="H1D0292ED54554F2A923E81B833516F10"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">The Commissioner, in coordination with the Administrator of the Small Business Administration, shall provide technical assistance, such as guidance and expertise, to small businesses regarding compliance with the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, including the amendments made by such Act.</text>
</subsection><subsection id="H2C2EA067F58840DF87AED835C234DDE6"><enum>(b)</enum><header>Compliance guide</header><text>Not later than 180 days after the date of the enactment of <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, the Secretary shall issue a small business guide setting forth in plain language the requirements of sections 605 and 606 in order to assist small businesses in complying with such requirements.</text></subsection></section><after-quoted-block>. </after-quoted-block></quoted-block>
</section><section commented="no" id="H5E63456520404D95882A9702D3BC9B3E"><enum>109.</enum><header>Animal testing restrictions</header>
<subsection id="H3E30D78B5FBE45EDB7FC42430B429DB1"><enum>(a)</enum><header>In general</header><text>Section 601 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref>) is amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="HE464EF33CD13459AB29186A7AC053591" style="OLC">
<subsection id="HB12EAEBCB5284161A9469E310243E2FA"><enum>(f)</enum><text display-inline="yes-display-inline">If the cosmetic product, cosmetic formulation, or cosmetic ingredient was developed or manufactured using an animal test that was conducted or contracted by the manufacturer, or any affiliate or supplier of the manufacturer, unless one of the following applies:</text>
<paragraph id="HD291F9FF106047B3BEE3CFBFD4450393"><enum>(1)</enum><text display-inline="yes-display-inline">With respect to a cosmetic ingredient of the cosmetic product or cosmetic formulation, an animal test is required by the Secretary to evaluate the safety of such ingredient or formulation.</text>
</paragraph><paragraph id="H94C51B3DC944462999936762E1F37897"><enum>(2)</enum><text display-inline="yes-display-inline">With respect to a cosmetic ingredient of the cosmetic product or cosmetic formulation, the cosmetic ingredient or cosmetic formulation is in wide use and cannot be replaced by another ingredient that is capable of performing a similar function without posing a potentially greater risk to human health and there is not an alternative method for testing the cosmetic ingredient that is accepted by the Secretary and the Interagency Coordinating Committee on Validation of Alternative Methods.</text>
</paragraph><paragraph id="H7D2ECF4FB5E3431C88AEFA12B5DBFECD"><enum>(3)</enum><text>The animal test was conducted to comply with a requirement of another Federal agency or a State or foreign regulatory authority.</text>
</paragraph><paragraph id="HB083E34A789C4634857DD082EF645F76"><enum>(4)</enum><text display-inline="yes-display-inline">In the case of a cosmetic product, cosmetic formulation, or cosmetic ingredient that is also a drug, the animal test was conducted with respect to the approval under chapter V of the application submitted with respect to such product, formulation, or ingredient.</text>
</paragraph><paragraph id="H89FED6C81F0146DF8B6DEF4FC04352C4"><enum>(5)</enum><text>The animal test was conducted for purposes not related to developing or manufacturing the cosmetic product, cosmetic formulation, or cosmetic ingredient, and in response to a requirement of a Federal, State, or foreign regulatory authority.</text></paragraph></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection id="HDEEA77C717644DBF86ECC0D69981F87E"><enum>(b)</enum><header>Applicability</header><text display-inline="yes-display-inline">The amendment made by subsection (a) shall apply with respect to cosmetic products or cosmetic formulations introduced or delivered for introduction into interstate commerce on or after the date that is two years after the date of enactment of this Act. <italic></italic></text>
</subsection><subsection commented="no" id="HB273E648A23F4C3685F0539D0D8B97FC"><enum>(c)</enum><header>Guidance</header><text>Not later than 1 year after the date of enactment of this Act, the Secretary shall issue guidance on the acceptability of scientifically reliable and relevant alternatives to animal testing for the safety of cosmetic products, cosmetic formulations, and cosmetic ingredients, and encouraging the use of such methods.</text>
</subsection><subsection commented="no" id="H2D6F85B7CA6C46FD9402F488DF145191"><enum>(d)</enum><header>Resources regarding animal testing alternatives</header><text display-inline="yes-display-inline">Not later than 180 days after the date of enactment of this Act, the Secretary shall publish information on the internet website of the Food and Drug Administration regarding resources available for information about non-animal methods, and methods that reduce animal usage, in testing for the safety of cosmetic products, cosmetic formulations, and cosmetic ingredients.</text>
</subsection><subsection id="H02EE78AEE2CA48249B2E1E4EFFDB2B4E"><enum>(e)</enum><header>Rules of construction</header>
<paragraph id="HC6531EC5EA564DBEAC78A0A8EA9D004D"><enum>(1)</enum><header>Use of evidence</header><text display-inline="yes-display-inline">Nothing in this section, or the amendment made by this section, shall be construed to prohibit any entity from reviewing, assessing, or retaining evidence generated from animal testing.</text>
</paragraph><paragraph id="H57D0EA9314584F2EB2A5E2D203018E81"><enum>(2)</enum><header>Acceptance of data by Secretary</header><text display-inline="yes-display-inline">Nothing in this section, or the amendment made by this section, shall be construed to prohibit the Secretary from accepting data from animal testing conducted—</text>
<subparagraph id="HD59C194FB32F455D8260E4A30A7DD58B"><enum>(A)</enum><text>prior to the date specified in subsection (b); or</text> </subparagraph><subparagraph id="H10109E2AAEB64C1FAE83EA59480C1767"><enum>(B)</enum><text>on or after such date—</text>
<clause id="H63D0BAA7F5D3467280CDA94AC26B75D3"><enum>(i)</enum><text display-inline="yes-display-inline">in the case of a cosmetic product, cosmetic formulation, or cosmetic ingredient that is also a drug, with respect to the approval under chapter V of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/351">21 U.S.C. 351</external-xref> et seq.) of the application submitted with respect to such product, formulation, or ingredient; or</text>
</clause><clause id="H3E3E249D1D9E440E9972A592FFE5CA48"><enum>(ii)</enum><text display-inline="yes-display-inline">pursuant to requirements of a Federal, State, or foreign regulatory authority.</text> </clause></subparagraph></paragraph></subsection></section><section id="HD0795DF5C3D64375841EE3FA831912FD"><enum>110.</enum><header>Counterfeit cosmetics</header> <subsection id="H83F3BADA2AD2436EB09D423BB895EE37"><enum>(a)</enum><header>Counterfeit cosmetics defined</header><text display-inline="yes-display-inline">Section 201(i) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/321">21 U.S.C. 321(i)</external-xref>) is amended—</text>
<paragraph id="H8952828A712A4BD7919D90D1BA90D3B4"><enum>(1)</enum><text>by striking <quote>(i) The term</quote> inserting <quote>(i)(1) The term</quote>;</text> </paragraph><paragraph id="H138A06A863A9488F922778C0D69EFB0C"><enum>(2)</enum><text>by striking <quote>(1) articles intended to be</quote> and inserting <quote>(A) articles intended to be</quote>;</text>
</paragraph><paragraph id="H411958BDEA6A4F9A87DCBC6C8856DDE2"><enum>(3)</enum><text>by striking <quote>(2) articles intended for use</quote> and inserting <quote>(B) articles intended for use</quote>; and</text> </paragraph><paragraph id="H9EB08376F15B41678279375517C71D7A"><enum>(4)</enum><text display-inline="yes-display-inline">by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="HDE961739814F4E9290C7E54F7B14E824" style="traditional">
<paragraph id="HA55DD5694FEE44F8B5D48B690F97E9BF" indent="up1"><enum>(2)</enum><text display-inline="yes-display-inline">The term <term>counterfeit cosmetic</term> means a cosmetic which, or the container or labeling of which, without authorization—</text> <subparagraph id="H807CAC9D9B984C469D11ACF1B6B6DC23"><enum>(A)</enum><text>bears the trademark, trade name, or other identifying mark, imprint, or device, or any likeness thereof, of a cosmetic manufacturer, processor, packer, or distributor other than the person or persons who in fact manufactured, processed, packed, or distributed such cosmetic; and</text>
</subparagraph><subparagraph id="H84265942C6F94B748E9400521060140B"><enum>(B)</enum><text>thereby falsely purports or is represented to be the product of, or to have been packed or distributed by, such other cosmetic manufacturer, processor, packer, or distributor.</text></subparagraph></paragraph><after-quoted-block>.</after-quoted-block></quoted-block>
</paragraph></subsection><subsection id="H4F1198D72B2347A8849652897701164B"><enum>(b)</enum><header>Prohibited act</header><text>Section 301(i) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/331">21 U.S.C. 331(i)</external-xref>) is amended—</text> <paragraph id="HB8A1276DF74C4B4AB94CFACC9C3B07BD"><enum>(1)</enum><text>in subparagraph (2)—</text>
<subparagraph id="HD7A4FAA24F4F473AAC40B30F1F0ACAA6"><enum>(A)</enum><text>by inserting <quote>digital printer,</quote> after <quote>stone,</quote>;</text> </subparagraph><subparagraph id="H9063A7E1DE754C75995D1F77660D2E2F"><enum>(B)</enum><text>by inserting <quote>cosmetic</quote> after <quote>drug or</quote>; and</text>
</subparagraph><subparagraph id="HCC9C1DE0F5564808AD1FC4C0FB5DA901"><enum>(C)</enum><text>by inserting before the period at the end the following: <quote>or such cosmetic a counterfeit cosmetic</quote>; and</text> </subparagraph></paragraph><paragraph id="H85AD7B9DE3B04759AC8EAD87CD93D06A"><enum>(2)</enum><text>in subparagraph (3)—</text>
<subparagraph id="H5A345DE1360F4FFAA715D7263B325AA7"><enum>(A)</enum><text display-inline="yes-display-inline">by inserting <quote>or a cosmetic to be a counterfeit cosmetic</quote> after <quote>to be a counterfeit drug</quote>; and</text> </subparagraph><subparagraph id="HE44D17521D744B4CBF53AA93946CAE03"><enum>(B)</enum><text>by inserting <quote>or counterfeit cosmetic</quote> before the period at the end.</text>
</subparagraph></paragraph></subsection><subsection id="H7BC343F4F935489998D9DC07D4307EED"><enum>(c)</enum><header>Penalties</header><text display-inline="yes-display-inline">Section 303(c)(5) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/333">21 U.S.C. 333(c)(5)</external-xref>) is amended—</text> <paragraph id="HDACD95F878494012BC920C9487AE88F0"><enum>(1)</enum><text>by inserting <quote>digital printer</quote> after <quote>stone,</quote>;</text>
</paragraph><paragraph id="H3EC01E495A994B3FAB899D69C1FEEAFC"><enum>(2)</enum><text>by inserting <quote>or a cosmetic being a counterfeit cosmetic</quote> after <quote>drug being a counterfeit drug</quote>; and</text> </paragraph><paragraph id="HAB7EEDE4AC724953A39B2206185EDF17"><enum>(3)</enum><text display-inline="yes-display-inline">by inserting before the period at the end the following: <quote>or the cosmetic was a counterfeit cosmetic</quote>.</text>
</paragraph></subsection><subsection id="HE57B0A751822424884409086A938834C"><enum>(d)</enum><header>Seizure</header><text>Section 304(a)(2) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/334">21 U.S.C. 334(a)(2)</external-xref>) is amended—</text> <paragraph id="H671F421A19B44DC888DC23D1F18DCF96"><enum>(1)</enum><text>by striking <quote>(B) Any container</quote> and all that follows through <quote>(D) Any adulterated</quote> and inserting <quote>(B) Any cosmetic that is a counterfeit cosmetic, (C) Any container of a counterfeit drug or counterfeit cosmetic, (D) Any punch, die, plate, stone, labeling, container, digital printer, or other thing used or designed for use in making a counterfeit drug or drugs or a counterfeit cosmetic or cosmetics, (E) Any adulterated</quote>; and</text>
</paragraph><paragraph id="H8A01855438094362BDF487C0F5804BD0"><enum>(2)</enum><text>by striking <quote>(E)</quote> and inserting <quote>(F)</quote> before <quote>Any adulterated or misbranded tobacco product</quote>.</text> </paragraph></subsection><subsection id="H73F293CCB8934F8EB431D8C963C52437"><enum>(e)</enum><header>Examinations and investigations</header><text>Section 702(e) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/372">21 U.S.C. 372(e)</external-xref>) is amended—</text>
<paragraph id="H7CE7B03C5AD14F1BBA982FC83938E4DD"><enum>(1)</enum><text>in the matter preceding paragraph (1), by inserting <quote>or counterfeit cosmetics</quote> after <quote>counterfeit drugs</quote>;</text> </paragraph><paragraph id="H25A2753B57E149C6B4E6B2D7C6CC5008"><enum>(2)</enum><text>in paragraph (4), by inserting <quote>or cosmetics</quote> after <quote>such drugs</quote>; and</text>
</paragraph><paragraph id="H5E852AC8671D476D9237857E377377E9"><enum>(3)</enum><text>in paragraph (5)—</text> <subparagraph id="H2CB71DB609F649D1BE88FBEB1C9F0B62"><enum>(A)</enum><text>by striking <quote>drugs or containers</quote> and inserting <quote>drugs, cosmetics, or containers</quote>; and</text>
</subparagraph><subparagraph id="H781D57F3E21B4E06845C07543235C884"><enum>(B)</enum><text>by inserting <quote>digital printers,</quote> after <quote>labeling,</quote>.</text> </subparagraph></paragraph></subsection></section><section commented="no" id="H88BB4D858A404825A0CA0B1723353E6D"><enum>111.</enum><header>Foreign supplier verification</header> <subsection commented="no" display-inline="no-display-inline" id="H160F10F0E0154F1A83849005F2B0A3E9"><enum>(a)</enum><header>In general</header><text>Chapter VIII of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/381">21 U.S.C. 381</external-xref> et seq.) is amended by adding at the end the following:</text>
<quoted-block id="H68D45572317E4EE0906935848593FC0F" style="OLC">
<section commented="no" id="HAC8062595783461E80C7822F71C10D4D"><enum>810.</enum><header>Cosmetics foreign supplier verification program</header>
<subsection commented="no" id="H105E2964AF49427FBA0CD4157BFB3672"><enum>(a)</enum><header>In general</header>
<paragraph commented="no" id="HA3D199171AAD4C919A302FBA318BAE8F"><enum>(1)</enum><header>Verification requirement</header><text>Except as provided under subsection (e), each importer shall perform risk-based foreign supplier verification activities for the purpose of verifying that the cosmetic product or cosmetic ingredient imported by the importer (or agent thereof)—</text>
<subparagraph commented="no" id="HE16C0049BE8440C88719F5BAF70CDED7"><enum>(A)</enum><text>has been manufactured according to the cosmetic product good manufacturing practices established under section 610; and</text>
</subparagraph><subparagraph commented="no" id="HC6179AC8888D4324B7B9E1A5BBBD80BE"><enum>(B)</enum><text>is not adulterated under section 601 or misbranded under section 602.</text> </subparagraph></paragraph><paragraph commented="no" id="H892D3DD8D65B41809F60A13461BE7173"><enum>(2)</enum><header>Importer defined</header><text>For purposes of this section, the term <term>importer</term> means, with respect to a cosmetic product or cosmetic ingredient—</text>
<subparagraph commented="no" id="HE63DDFADB06E432C998F422BC9336229"><enum>(A)</enum><text>the United States owner or consignee of the cosmetic product or cosmetic ingredient at the time of entry of such cosmetic product or cosmetic ingredient into the United States; or</text>
</subparagraph><subparagraph commented="no" id="H405C28E5D69C4725AE3DD509631CC5BF"><enum>(B)</enum><text>in the case when there is no United States owner or consignee as described in subparagraph (A), the United States agent or representative of a foreign owner or consignee of the cosmetic product or cosmetic ingredient at the time of entry of such article into the United States.</text>
</subparagraph></paragraph></subsection><subsection commented="no" id="HF0B53A5054C34182A5D961234B22249A"><enum>(b)</enum><header>Guidance</header><text>Not later than 1 year after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, the Secretary shall issue guidance to assist importers in developing foreign supplier verification programs.</text>
</subsection><subsection commented="no" id="H4E8A8538336B4008B91D0FDE35BD3B2B"><enum>(c)</enum><header>Regulations</header>
<paragraph commented="no" id="H0EA69B952C5D4566BF222ED01E3B3815"><enum>(1)</enum><header>In general</header><text>Not later than 1 year after the date of enactment of <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, the Secretary shall promulgate regulations to provide for the content of the foreign supplier verification program established under subsection (a).</text>
</paragraph><paragraph commented="no" id="H640C0C354A354FF7AE2B2069FF53FB59"><enum>(2)</enum><header>Requirements</header><text>The regulations promulgated under paragraph (1)—</text> <subparagraph commented="no" id="H76A1D72ACC6E406998EA6194798FE501"><enum>(A)</enum><text>shall require that the foreign supplier verification program of each importer be adequate to provide assurances that each foreign supplier to the importer produces the imported cosmetic product or cosmetic ingredient in compliance with—</text>
<clause commented="no" id="H8C38024B4A23417CB4C19341880F38D9"><enum>(i)</enum><text>with cosmetic good manufacturing practices established under section 610; and</text> </clause><clause commented="no" id="HC3752260242841468F1E2CBFB2A18DC7"><enum>(ii)</enum><text>sections 601 and 602; and</text>
</clause></subparagraph><subparagraph commented="no" id="HE74E94676A9D422E88046D8C20275282"><enum>(B)</enum><text>shall include such other requirements as the Secretary deems necessary and appropriate to verify that cosmetic products and cosmetic ingredients imported into the United States are as safe as cosmetic products and cosmetic ingredients produced and sold within the United States.</text>
</subparagraph></paragraph><paragraph commented="no" id="HF53C0F9C7F544B7E975A7F8614516400"><enum>(3)</enum><header>Considerations</header><text>In promulgating regulations under this subsection, the Secretary shall, as appropriate, take into account differences among importers and types of imported cosmetic products and cosmetic ingredients, including based on the level of risk posed by the imported cosmetic product or cosmetic ingredient.</text>
</paragraph><paragraph commented="no" id="H9FC2B2DF9FF148C6AC87BBBED7D1F85E"><enum>(4)</enum><header>Activities</header><text>Verification activities under a foreign supplier verification program under this section may include monitoring records for shipments, lot-by-lot certification of compliance, annual on-site inspections, compliance with cosmetic good manufacturing practices and other safety processes, and periodically testing and sampling shipments.</text>
</paragraph></subsection><subsection commented="no" id="H478ECF139D2D4F4D8BBFF03CFA83B1E4"><enum>(d)</enum><header>Record maintenance and access</header><text>Records of an importer related to a foreign supplier verification program shall—</text> <paragraph commented="no" id="H5E99A259C4074ECCAE6FA6FE7F4F0000"><enum>(1)</enum><text>be maintained for a period of not less than 2 years; and</text>
</paragraph><paragraph commented="no" id="H073431E1C0D64FFBB6C9EE1B84AD0731"><enum>(2)</enum><text>be made available promptly to a duly authorized representative of the Secretary upon request.</text> </paragraph></subsection><subsection commented="no" id="HE87750CC226E4C5CB178316AA844F326"><enum>(e)</enum><header>Exemptions</header><text>The Secretary, by notice published in the Federal Register, shall establish an exemption from the requirements of this section for cosmetic products or cosmetic ingredients imported in small quantities for research and evaluation purposes or for personal consumption, provided that such cosmetic products or cosmetic ingredients are not intended for retail sale and are not sold or distributed to the public.</text>
</subsection><subsection commented="no" id="H2B95116E370C4941912E241555B50180"><enum>(f)</enum><header>Publication of list of participants</header><text>The Secretary shall publish and maintain on the internet website of the Food and Drug Administration a current list that includes the name of, location of, and other information deemed necessary by the Secretary about, importers participating under this section.</text></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection commented="no" id="H3886A2F011D9407E8E162DCE4A0A50C2"><enum>(b)</enum><header>Prohibited act</header><text>Section 301 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/331">21 U.S.C. 331</external-xref>), as amended by section 113, is further amended by adding at the end the following:</text>
<quoted-block id="HF30A4B3557FA4DA7BE7E0B16EC8DD9CA" style="OLC">
<subsection commented="no" id="H3649F20194A64996BFC5A096A97D477B"><enum>(ggg)</enum><text>The importation or offering for importation of a cosmetic product or cosmetic ingredient if the importer (as defined in section 810) does not have in place a foreign supplier verification program in compliance with such section 810.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
</subsection><subsection id="H909B4B18E1304320A198339629A3686E"><enum>(c)</enum><header>Imports</header><text display-inline="yes-display-inline">Section 801(a) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/381">21 U.S.C. 381(a)</external-xref>) is amended by striking <quote>or the importer (as defined in section 805) is in violation of such section 805</quote> and inserting <quote>, or being imported or offered for import into the United States by an importer (as defined in section 805 or 810, as applicable) that is in violation of section 805 or 810, respectively</quote>.</text>
</subsection><subsection commented="no" id="H66ECB3CDA0E64BE585DBC261C4EEC67B"><enum>(d)</enum><header>Effective date</header><text>The amendments made by this section shall take effect 2 years after the date of enactment of this Act.</text>
</subsection></section><section id="H183DABB0779E45F98863D5DB7A1CE604"><enum>112.</enum><header>Applicability with respect to certain cosmetics</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 108, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H45372DC651864E628ED745D702926C94" style="OLC">
<section id="H89F4B1E94EAD4FA59FF027038549669C"><enum>617.</enum><header>Applicability with respect to certain cosmetics</header><text display-inline="no-display-inline">In the case of a cosmetic product or a facility that is subject to the requirements under this chapter and chapter V, if any requirement under chapter V with respect to such cosmetic or facility is substantially similar to a requirement under this chapter, the cosmetic product or facility shall be deemed to be in compliance with the applicable requirement under this chapter if such product or facility is in compliance with such substantially similar requirement under chapter V, provided that the product or facility has not obtained a waiver from the requirement under chapter V.</text></section><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section commented="no" id="H98FECD6B5E66438684A145609D372013"><enum>113.</enum><header>Saving clause</header><text display-inline="no-display-inline">Chapter VI of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref> et seq.), as amended by section 112, is further amended by adding the following:</text>
<quoted-block display-inline="no-display-inline" id="H0C5A25E407004632841FBC53B4D54BF2" style="OLC">
<section commented="no" id="H73293F2913A04EB19435EEE3B4EDAE4C"><enum>616.</enum><header>Savings clause</header><text display-inline="no-display-inline">Nothing in the amendments to this Act made by the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, nor any standard, rule, requirement, regulation, adverse event report, safety assessment, safety determination, scientific assessment, or order issued or implemented pursuant to such amendments, shall be construed to modify or otherwise affect, preempt, or displace any cause of action or State or Federal law creating a remedy for civil relief or criminal cause of action, whether statutory or based in common law.</text></section><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section commented="no" id="HE8D1E8DF1F10417C8DD4E77C8CF341B5"><enum>114.</enum><header>Enforcement</header>
<subsection commented="no" id="H88110D89AE3346B5A43F78B6E1CA4786"><enum>(a)</enum><header>Prohibited acts</header><text display-inline="yes-display-inline">Section 301 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/331">21 U.S.C. 331</external-xref>) is amended—</text> <paragraph commented="no" id="H82B21CDBCD2A4634A37ECE33B0B6BF1B"><enum>(1)</enum><text>in paragraph (e)—</text>
<subparagraph commented="no" id="HD4C82343B232469EABCB9EFC209A788A"><enum>(A)</enum><text>by striking <quote>504, 564,</quote> and inserting <quote>504, 564, 611, 612</quote>; and</text> </subparagraph><subparagraph commented="no" id="HCF53C0438EC049A3879114B7E91032D1"><enum>(B)</enum><text>by striking <quote>519, 564,</quote> and inserting <quote>519, 564, 609, 611,</quote>;</text>
</subparagraph></paragraph><paragraph commented="no" id="H565CB0B0FA164B6D814604F50E5FCE8A"><enum>(2)</enum><text>in paragraph (j) by inserting <quote>607, 608, 610, 611</quote> before <quote>704</quote>;</text> </paragraph><paragraph commented="no" id="H5A9A353463544092977CCA9D987FB00D"><enum>(3)</enum><text>in paragraph (ii)—</text>
<subparagraph commented="no" id="HB9EA089114D2439B945B34DFD91E73E7"><enum>(A)</enum><text>by striking <quote>760 or 761)</quote> and inserting <quote>604, 760, or 761)</quote>; and</text> </subparagraph><subparagraph commented="no" id="HF8021753C86A4E7894732BC53D9E913A"><enum>(B)</enum><text>by striking <quote>760 or 761) submitted</quote> and inserting <quote>611, 760, or 761) submitted</quote>;</text>
</subparagraph></paragraph><paragraph commented="no" id="H01B242557611439FAF664618C5443BB7"><enum>(4)</enum><text>in paragraph (xx), by inserting <quote>or 613</quote> after <quote>423</quote>; and</text> </paragraph><paragraph commented="no" id="HA46D970672BD460EAFC87436F7FB9E96"><enum>(5)</enum><text>by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H50AED28483E64ED595B65263FA6ED1BC" style="OLC">
<subsection commented="no" id="HC2EBC0DC34A7406E8789CE034E7300E5"><enum>(fff)</enum><text>The failure to register in accordance with section 605, the failure to submit a cosmetic ingredient statement under section 606, the failure to provide information required by section 605 or 606, or the failure to update the information required by section 605 or 606, as required.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
</paragraph></subsection><subsection commented="no" id="H9EF3B536DB784F4CA92CBCCFB2C3455F"><enum>(b)</enum><header>Adulteration</header><text>Section 601 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/361">21 U.S.C. 361</external-xref>), as amended by section 603, is further amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H40C067FD5F7142F3BC2377E37EADF42E" style="OLC">
<subsection commented="no" id="H55D08C9572714CDFBEBC52F724F57EF5"><enum>(g)</enum><text>If it contains, after the date prescribed under section 608(d)(3), an ingredient that the Secretary has determined under section 608(d)(4) to be not safe, or not safe under the conditions of use recommended or suggested in the label based on an order issued by the Secretary under section 608(d)(4).</text>
</subsection><subsection commented="no" id="H641725F29D6A4AB596ADFAEF4D94CC21"><enum>(h)</enum><text>If it is a cosmetic product for which any requirement of section 609 is not met.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block> </subsection><subsection commented="no" id="HC94B178B4CE54B56B57462BF48492D24"><enum>(c)</enum><header>Misbranding</header><text display-inline="yes-display-inline">Section 602 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/362">21 U.S.C. 362</external-xref>), as amended by section 106, is further amended—</text>
<paragraph commented="no" id="H35091D6203174575B0A4E299073E2FAF"><enum>(1)</enum><text>in paragraph (b)—</text> <subparagraph commented="no" id="H34E9EF3CE10C44088EAE8252E0E4EDAE"><enum>(A)</enum><text>by striking <quote>and (2)</quote> and inserting <quote>(2)</quote>; and</text>
</subparagraph><subparagraph commented="no" id="HFC03CA0CCBBF40C3A12FB00CDA329155"><enum>(B)</enum><text>by inserting <quote>; and (3) a domestic address or a domestic telephone number, or electronic contact information, through which the responsible person may receive a report of an adverse event associated with the use of such cosmetic product</quote> after <quote>numerical count</quote>; and</text>
</subparagraph></paragraph><paragraph commented="no" id="HFAB43BF760A34E71822C386F25B15D4C"><enum>(2)</enum><text>by adding at the end the following:</text> <quoted-block display-inline="no-display-inline" id="H1B980D8351B84CFF8E70BC9DEDC985DE" style="OLC"> <subsection commented="no" id="H5759FF0485A541DEB3ACDFCE73DA9A17"><enum>(h)</enum><text>If it is a cosmetic product and it has been manufactured, processed, packed, or held in any factory, warehouse, or establishment and the responsible person delays, denies, or limits an inspection, or refuses to permit entry or inspection.</text>
</subsection><subsection id="H5107837F79E64D2DA8AA1EA3947BA564"><enum>(i)</enum><text display-inline="yes-display-inline">If a fragrance ingredient described in section 615 is not disclosed to consumers through a method identified by the Food and Drug Administration in the guidance document issued under such section.</text>
</subsection><subsection commented="no" id="HEDD6C9A02DB3467EB3A81935C29CE005"><enum>(j)</enum><text>If its labeling does not conform with a requirement under section 614.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block> </paragraph></subsection><subsection commented="no" id="H8F4898F07D074AF996E029CD374A88BA"><enum>(d)</enum><header>Guidance</header><text display-inline="yes-display-inline">Not later than 1 year after the date of enactment of this Act, the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall issue guidance that defines the circumstances that would constitute delaying, denying, or limiting inspection, or refusing to permit entry or inspection, for purposes of section 602(g) of the Federal Food, Drug, and Cosmetic Act, as added by subsection (c)(2).</text>
</subsection><subsection commented="no" id="H2FE61503210D4A84A717C004F84A6CB1"><enum>(e)</enum><header>Imports</header><text display-inline="yes-display-inline">Section 801(a) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/381">21 U.S.C. 381(a)</external-xref>) is amended—</text> <paragraph commented="no" id="H495B018C594C4FC9AC9B195193C8EA13"><enum>(1)</enum><text>by striking <quote>section 760 or 761</quote> the first, third, and fourth place such term appears and inserting <quote>section 611, 760, or 761</quote>; and</text>
</paragraph><paragraph commented="no" id="H0AC3296E89564FE8A4E2C6E4EC268D30"><enum>(2)</enum><text>by striking <quote>760 or 761)</quote> and inserting <quote>604, 760, or 761)</quote>.</text> </paragraph></subsection><subsection commented="no" id="H852754BAA7F04371A8C9AE7861CDE687"><enum>(f)</enum><header>Facility inspection</header><text display-inline="yes-display-inline">Section 704(a)(1) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/374">21 U.S.C. 374(a)(1)</external-xref>) is amended by inserting after the third sentence the following: <quote>In the case of any person who manufactures, processes, packs, holds, distributes, or imports a cosmetic product, or distributes a cosmetic product and affixes its name on the cosmetic label, the inspection shall extend to all records and other information <italic></italic>described in section 612 (regarding inspection of cosmetic records), subject to the limitations under of such section.</quote>.</text>
</subsection></section><enum>II</enum><header>Fees Related to Cosmetic Products</header>
<section commented="no" id="HF347D518C8264ACDA7EBA09FF3B60896"><enum>201.</enum><header>Findings</header><text display-inline="no-display-inline">The Congress finds that the fees authorized by the amendment made by section 202 of this Act will be dedicated to cosmetic safety activities, as defined in section 744L of the Federal Food, Drug, and Cosmetic Act, as added by such section 202. Such fees should supplement, not supplant, funding dedicated to cosmetic safety activities of the Food and Drug Administration. Future fees authorized by the reauthorization of part 10 of subchapter C of chapter VII of the Federal Food, Drug, and Cosmetic Act to be collected by the Secretary of Health and Human Services should be dedicated to cosmetic safety activities as set forth in the goals identified for purposes of such part 10, in the letters from the Secretary of Health and Human Services to the Chairman of the Committee on Health, Education, Labor, and Pensions of the Senate and the Chairman of the Committee on Energy and Commerce of the House of Representatives, as set forth in the Congressional Record.</text>
</section><section commented="no" id="H5E3BB5B8D3154E4DBDED7275329C4F9D"><enum>202.</enum><header>Authority to assess and use cosmetic product fees</header><text display-inline="no-display-inline">Subchapter C of chapter VII of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/379f">21 U.S.C. 379f</external-xref> et seq.) is amended by adding at the end the following:</text>
<quoted-block display-inline="no-display-inline" id="H50876C2BFD394D6E9B8A54C24E149206" style="OLC">
<part commented="no" id="H3F207D897CA3439695DD7C1EF558F318" style="OLC"><enum>10</enum><header>Fees Relating to Cosmetic Products</header>
<section commented="no" id="H53BC787B89D147F7A696310EDA2F3CDC"><enum>744L.</enum><header>Definitions</header><text display-inline="no-display-inline">For the purposes of this part:</text> <paragraph commented="no" id="HA6D7CD314D624CF89B66B62B269ABCAD"><enum>(1)</enum><header>Adjustment factor</header><text display-inline="yes-display-inline">The term <term>adjustment factor</term> applicable to a fiscal year means the Consumer Price Index for all urban consumers (all items; United States city average) for October of the preceding fiscal year divided by such index for October 2018.</text>
</paragraph><paragraph id="HCDE4CA19FE164424A6F3E98D5AB553B8"><enum>(2)</enum><header>Cosmetic formulation</header><text>The term <term>cosmetic formulation</term> has the meaning given to such term in section 604.</text> </paragraph><paragraph commented="no" id="H9D300B73123849EF8AAF87F6CC2B089A"><enum>(3)</enum><header>Contract manufacturer</header><text>The term <term>contract manufacturer</term> means a cosmetic manufacturer where neither the owner, operator, or agent in charge of such entity nor any affiliate of such owner, operator, or agent in charge sells the cosmetic ingredient, cosmetic formulation, or cosmetic product unless there is a specific contractual agreement in place.</text>
</paragraph><paragraph commented="no" id="H894D7542A0704EC8A3A457071B76C47C"><enum>(4)</enum><header>Cosmetic product</header><text>The term <term>cosmetic product</term> has the meaning given to such term in section 604.</text> </paragraph><paragraph commented="no" id="HBEAF2BC3C8DC4558B87E414B18AF2DBE"><enum>(5)</enum><header>Cosmetic safety activities</header><text>The term <term>cosmetic safety activities</term>—</text>
<subparagraph commented="no" id="H75E0E5F8B0084D2A90913BE52E26DEB5"><enum>(A)</enum><text>means activities of the Secretary related to compliance by responsible persons required to register under section 605 with respect to cosmetics, including administrative activities, such as—</text>
<clause commented="no" id="H366A738C00B04FF19ABE79B6FB65E0EE"><enum>(i)</enum><text>information technology acquisition, management, maintenance, and support;</text> </clause><clause commented="no" id="H0C8D90E23F914963ACC3B81943A164F9"><enum>(ii)</enum><text>the acquisition, administration, and maintenance of the cosmetic registration system under section 605 and the cosmetic ingredient statement system under section 606;</text>
</clause><clause commented="no" id="H09045504B9654A2A99E29BF8131D579F"><enum>(iii)</enum><text>fee assessment and collection under this part; and</text> </clause><clause commented="no" id="H1B5A87218AF54795808867E0F2F08174"><enum>(iv)</enum><text>the acquisition, leasing, maintenance, renovation, and repair of facilities, fixtures, furniture, scientific equipment, and other necessary materials and supplies for purposes of clauses (i) through (iii);</text>
</clause></subparagraph><subparagraph commented="no" id="H2E2349D0A18D41F1B5E55F8E9F7723B5"><enum>(B)</enum><text>includes activities of the Secretary related to implementation of section 608, regarding the review of cosmetic ingredients and nonfunctional constituents;</text>
</subparagraph><subparagraph commented="no" id="H6FCFD2D2BDB64131B217192C8BF817D4"><enum>(C)</enum><text>includes activities of the Secretary related to implementation of section 606;</text> </subparagraph><subparagraph commented="no" id="H525AA23D009B4A028F26D7340B3A6669"><enum>(D)</enum><text>includes activities of the Secretary related to implementation and enforcement, such as the establishment of good manufacturing practices, the review of adverse event reports, inspection planning and inspections, and use of enforcement tools; and</text>
</subparagraph><subparagraph id="H4A2C0D1CCEE14C49AC8F54F8DEBD5617"><enum>(E)</enum><text display-inline="yes-display-inline">includes activities of the Secretary related to meetings with regulated industry regarding determinations under section 608.</text>
</subparagraph></paragraph><paragraph commented="no" id="H0D31F6102C8847AD8E956DE6D9BE28E5"><enum>(6)</enum><header>Gross annual sales</header><text display-inline="yes-display-inline">The term <term>gross annual sales</term> means the average United States gross annual sales for the previous 3 fiscal years of cosmetic products for a responsible person, including the sales of cosmetic products of all of its affiliates, as reported in the registration under section 605.</text>
</paragraph><paragraph commented="no" id="HFE59DCB516384BBB943C5E8ED1CA5FF5"><enum>(7)</enum><header>Large manufacturer</header><text>The term <term>large manufacturer</term> means any entity that manufactures cosmetic products or cosmetic formulations for sale or distribution in the United States and has gross annual sales of over $500,000,000.</text>
</paragraph><paragraph commented="no" id="H085D3F1520CA49498831183EB351BA18"><enum>(8)</enum><header>Midsize manufacturer</header><text>The term <term>midsize manufacturer</term> means any entity that manufactures cosmetic products or cosmetic formulations for sale or distribution in the United States and has gross annual sales that are not more than $500,000,000 and over $30,000,000.</text>
</paragraph><paragraph commented="no" id="HC325A233C2F64AFB9B0764D0C483D219"><enum>(9)</enum><header>Small manufacturer</header><text>The term <term>small manufacturer</term> means any entity that manufactures cosmetic products or cosmetic formulations for sale or distribution in the United States and has gross annual sales that are not more than $30,000,000 and over $1,000,000.</text>
</paragraph><paragraph commented="no" id="HD57974898CF347D7923BBDC9F82693EB"><enum>(10)</enum><header>Responsible person</header><text display-inline="yes-display-inline">The term <term>responsible person</term> means the owner, operator, agent in charge, or affiliate that owns the brand under which a cosmetic product is sold.</text>
</paragraph></section><section commented="no" id="H1037AED0E4FD4D87A1A427C5ECEEE1EB"><enum>744M.</enum><header>Registration fee</header>
<subsection commented="no" id="H8F637975294B4358A55B7A063824A026"><enum>(a)</enum><header>Assessment and collection</header>
<paragraph commented="no" id="HBA57F96F335743B9B155F63C84513BB3"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">Beginning in fiscal year 2020, the Secretary shall in accordance with this section assess and collect an annual fee from every responsible person that manufactures or distributes cosmetic products or cosmetic formulations in the United States.</text>
</paragraph><paragraph commented="no" id="HCA47FBCC187B421298B96FA0E6AF4679"><enum>(2)</enum><header>Payable date</header><text>Fees under this section shall be due and payable—</text> <subparagraph commented="no" id="H6342FDE7937E4304B488D6D51AA2980E"><enum>(A)</enum><text>for fiscal year 2020, with respect to responsible persons as described in paragraph (1) for such first program year, on the date that is 180 days after the identification in subsection (b); and</text>
</subparagraph><subparagraph commented="no" id="H9A1BF13AEC664C45A9EB5B9FA9C30E57"><enum>(B)</enum><text>for fiscal year 2021 and each subsequent fiscal year, on the later of—</text> <clause commented="no" id="HB1536C2DEE31443697FC415A358F9F34"><enum>(i)</enum><text>the date of registration or registration renewal, as applicable, under section 605; or</text>
</clause><clause commented="no" id="H69D46534AB8540E9A4D9023CE024DAA9"><enum>(ii)</enum><text>the date of enactment of an appropriations Act providing for the collection and obligation of fees under this section for the fiscal year involved.</text>
</clause></subparagraph></paragraph></subsection><subsection commented="no" id="H583A602F6F654013A23E63BE3B87606C"><enum>(b)</enum><header>One-Time identification of responsible persons for purposes of apportioning fees</header>
<paragraph commented="no" id="H5D7C66BCDA054428B0D6AB15932DDF07"><enum>(1)</enum><header>Required identification of responsible persons</header><text>Not later than 120 days after enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>, each responsible person that markets or sells a cosmetic product shall submit to the Secretary the information required under this subsection.</text>
</paragraph><paragraph commented="no" id="H1FB0EDA3A4E540A09CD33886DC6E962D"><enum>(2)</enum><header>Information required to be submitted</header><text>At a minimum, the submission required by paragraph (1) shall include for each such responsible person—</text>
<subparagraph commented="no" id="HC6884287958A49F886EDD95C761756FE"><enum>(A)</enum><text>the gross annual sales of cosmetic products or cosmetic formulations for the previous 3 fiscal years as will be reported in the first registration under section 605 for such responsible person, and an assessment of whether such responsible person qualifies as a small, midsize, or large manufacturer for the purposes of subsection (c)(3)(A);</text>
</subparagraph><subparagraph commented="no" id="H57578EA90C414EB295B738330B893BEF"><enum>(B)</enum><text>identification of facilities where such responsible person’s cosmetic products or cosmetic formulations are manufactured, which cosmetic products or cosmetic formulations are manufactured there, and any other products regulated under this Act that the facility manufactures;</text>
</subparagraph><subparagraph commented="no" id="H7691C966E9F04106950FB59DD9B85F96"><enum>(C)</enum><text>the location of all such facilities identified in subparagraph (B); and</text> </subparagraph><subparagraph commented="no" id="HE0E37844534F48118166CBB9C0A05166"><enum>(D)</enum><text>whether the facility is owned and operated by a contract manufacturer.</text>
</subparagraph></paragraph><paragraph commented="no" id="HD4C4D5E9EF6B46109C09D4062DFD01F3"><enum>(3)</enum><header>Notice</header><text display-inline="yes-display-inline">The Secretary may, by notice published in the Federal Register, specify the means and format for submission of the information under paragraph (2) and may specify, as necessary for purposes of this section, any additional information relevant to setting the annual fee under this section to be submitted.</text>
</paragraph></subsection><subsection commented="no" id="H2EB5B9ABA7C74A9CBDFA8DA3977638C3"><enum>(c)</enum><header>Fee setting and amounts</header>
<paragraph commented="no" id="HBC6468DB58C247ECA874F2EFB69121AC"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">Subject to subsection (d), the Secretary shall establish the fees to be collected under this section for each fiscal year beginning in fiscal year 2020, based on the methodology described in paragraph (3)(A), and shall publish such fees in each fiscal year after fiscal year 2020 in a Federal Register notice not later than 60 days before the beginning of each such fiscal year. For fiscal year 2020, the Secretary shall publish the fees 150 days after the date of enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>.</text>
</paragraph><paragraph commented="no" id="HE907C48F12894AF4927D15189A47847A"><enum>(2)</enum><header>Fee exemption</header><text display-inline="yes-display-inline">Any facility required to register under section 605 whose average gross annual sales of cosmetic products in the 3 fiscal years immediately preceding the fiscal year for which the annual fee will be paid was not more than $1,000,000, shall be exempt from registration fees under this section for that fiscal year.</text>
</paragraph><paragraph commented="no" id="H47F6CE7922DB41ECAD332493BF9A0130"><enum>(3)</enum><header>Annual fee setting</header>
<subparagraph commented="no" id="HE30346275635449891E5EA9249B8D7B3"><enum>(A)</enum><header>Fee setting</header><text>For fiscal years 2020 to 2027, the amount of the registration fee under subsection (a) shall be apportioned as follows:</text>
<clause commented="no" id="HF3C3A47309BB4EBE944C133F2A51E886"><enum>(i)</enum><text>Seventy percent shall be derived from fees from large manufacturers.</text> </clause><clause commented="no" id="HB3BF09E830634D2B829C8D3A83F9A6B0"><enum>(ii)</enum><text>Twenty percent shall be derived from fees from midsize manufacturers.</text>
</clause><clause commented="no" id="HAFD28A53F90B4574A74BF3B6F71CFA8A"><enum>(iii)</enum><text>Ten percent shall be derived from fees from small manufacturers.</text> </clause></subparagraph><subparagraph commented="no" id="HFD8A97280873454795106AF26982E30F"><enum>(B)</enum><header>Total revenue</header><text>The Secretary shall establish the fee amounts for each fiscal year in accordance with subparagraph (A), in order to generate a total estimated revenue of—</text>
<clause commented="no" id="H149AFC64022147D0B0C5117F0CA178C4"><enum>(i)</enum><text>$10,000,000 for fiscal year 2020;</text> </clause><clause commented="no" id="H7FE06A51DBCC48C6864D324B600129E1"><enum>(ii)</enum><text>$20,000,000 for fiscal year 2021;</text>
</clause><clause commented="no" id="H0A23AD24B7224051AB569391D44EF627"><enum>(iii)</enum><text>$35,000,000 for fiscal year 2022; and</text> </clause><clause commented="no" id="H4C7CC2EEDD5F461EA21F56F1E44D6354"><enum>(iv)</enum><text>$46,000,000 for each of fiscal years 2023 through 2027.</text>
</clause></subparagraph></paragraph></subsection><subsection commented="no" id="H26C8AED6BAF64FA89ADF521093186C8D"><enum>(d)</enum><header>Adjustments</header>
<paragraph commented="no" id="H2D48DFDF11254CD4BA0FA578A413A07A"><enum>(1)</enum><header>Inflation adjustments</header>
<subparagraph commented="no" id="H201C47C264BF495E89F8D9370E50EDAB"><enum>(A)</enum><header>Adjustment to total revenue amounts</header><text>For fiscal year 2020 and each subsequent fiscal year, the Secretary shall adjust the total revenue amount specified in subsection (c)(3) for such fiscal year by multiplying such amount by the applicable inflation adjustment under subparagraph (B) for such year.</text>
</subparagraph><subparagraph commented="no" id="H71FB4DDBC54644858257D95834C86E4D"><enum>(B)</enum><header>Applicable inflation adjustment</header><text>The applicable inflation adjustment for fiscal year 2022 and each subsequent fiscal year is the product of—</text>
<clause commented="no" id="HE3FEA06F8E94450A96F785BF79F0679C"><enum>(i)</enum><text>the base inflation adjustment under subparagraph (C) for such fiscal year; and</text> </clause><clause commented="no" id="H023D8645812445C5A3DAC3F693B491B4"><enum>(ii)</enum><text>the product of the base inflation adjustment under subparagraph (C) for each of the fiscal years preceding such fiscal year, beginning with fiscal year 2020.</text>
</clause></subparagraph><subparagraph commented="no" id="HCB418B5487AB46BFBE13145B04150F61"><enum>(C)</enum><header>Base inflation adjustment</header>
<clause commented="no" display-inline="no-display-inline" id="HB651E8EBC1AC4DD299E333A182FE5E16"><enum>(i)</enum><header>In general</header><text>Subject to further adjustment under clause (ii), the base inflation adjustment for a fiscal year is the sum of one plus—</text>
<subclause commented="no" id="HA8D2C1231E6A47A9B56F6AD8AA57C73F"><enum>(I)</enum><text>the average annual percent change in the cost, per full-time equivalent position of the Food and Drug Administration, of all personnel compensation and benefits paid with respect to such positions for the first 3 fiscal years of the preceding 4 fiscal years, multiplied by 0.60; and</text>
</subclause><subclause commented="no" id="HCC146FF2AFA44882B4F14805A49045D8"><enum>(II)</enum><text>the average annual percent change that occurred in the Consumer Price Index for urban consumers (Washington-Arlington-Alexandria; Not Seasonally Adjusted; All items; Annual Index) for the first 3 fiscal years of the preceding 4 years of available data multiplied by 0.40.</text>
</subclause></clause><clause commented="no" id="H7DA1D9B1154B4974A32F432E7645411C"><enum>(ii)</enum><header>Limitations</header><text>For purposes of subparagraph (B), if the base inflation adjustment for a fiscal year under clause (i)—</text>
<subclause commented="no" id="H1BCE86F45C114997BC3FEE497882610C"><enum>(I)</enum><text>is less than 1, such adjustment shall be considered to be equal to 1; or</text> </subclause><subclause commented="no" id="H8A9A43A747874F6DB8024D3B18D3A891"><enum>(II)</enum><text>is greater than 1.04, such adjustment shall be considered to be equal to 1.04.</text>
</subclause></clause></subparagraph></paragraph><paragraph commented="no" id="H9A6BCE84B3854F28A0BE0490DB152F65"><enum>(2)</enum><header>Final year adjustment</header><text>For fiscal year 2027, the Secretary may, in addition to adjustments under paragraph (1), further increase the fee revenues and fees established in subsection (c) if such an adjustment is necessary to provide for not more than 3 months of operating reserves of carryover fees for cosmetic safety activities for the first 3 months of fiscal year 2028. If such an adjustment is necessary, the rationale for the increase shall be contained in the annual Federal Register notice establishing fees for fiscal year 2027. If the Food and Drug Administration has carryover balances for such activities in excess of 3 months of such operating reserves, the adjustment under this paragraph shall not be made.</text>
</paragraph></subsection><subsection commented="no" id="HF3095FA41FE04F71BAF3F0281A4BE4A9"><enum>(e)</enum><header>Limitations</header>
<paragraph commented="no" id="H424C1DD3B3054363829A5871187D0CAE"><enum>(1)</enum><header>In general</header><text display-inline="yes-display-inline">With respect to the amount that is appropriated for a fiscal year for the cosmetics program of the Center for Food Safety and Applied Nutrition of the Food and Drug Administration and related field activities, fees may not be assessed under subsection (a) for the fiscal year unless the amount so appropriated (excluding the amount of fees appropriated for the fiscal year), is equal to or greater than the amount that is appropriated for such program for fiscal year 2019, multiplied by the adjustment factor applicable to the fiscal year involved. If the amount so appropriated prevents the Secretary from assessing fees under subsection (a), the Secretary is not required to carry out any activities described in section 608 during that fiscal year.</text>
</paragraph><paragraph commented="no" id="HB498B516054A47D1B052ACCE5FAD7210"><enum>(2)</enum><header>Authority</header><text>If the Secretary does not assess fees under subsection (a) during any portion of a fiscal year because of paragraph (1) and if at a later date in such fiscal year the Secretary may assess such fees, the Secretary may assess and collect such fees, without any modification in the rate, for registration under section 605 at any time in such fiscal year.</text>
</paragraph></subsection><subsection commented="no" id="H211459376A6F44C7895578596F726D02"><enum>(f)</enum><header>Crediting and availability of fees</header>
<paragraph commented="no" id="HEA58C5EB0116471F84045E7AE10A7B1B"><enum>(1)</enum><header>In general</header><text>Fees authorized under subsection (a) shall be collected and available for obligation only to the extent and in the amount provided in advance in appropriations Acts. Such fees are authorized to remain available until expended. Such sums as may be necessary may be transferred from the Food and Drug Administration salaries and expenses appropriation account without fiscal year limitation to such appropriation account for salaries and expenses with such fiscal year limitation. The sums transferred shall be available solely for cosmetic safety activities.</text>
</paragraph><paragraph commented="no" id="HEADC04A020FA4583A6CDDF3667BB29D3"><enum>(2)</enum><header>Collections and appropriations Acts</header>
<subparagraph commented="no" id="HCEC15AB0EEF444E98E949AF265B2DD78"><enum>(A)</enum><header>In general</header><text>Subject to subparagraphs (C) and (D), the fees authorized by this section shall be collected and available in each fiscal year in an amount not to exceed the amount specified in appropriation Acts, or otherwise made available for obligation, for such fiscal year.</text>
</subparagraph><subparagraph commented="no" id="H52FC387BD1904D5EAAA9161BC628CD33"><enum>(B)</enum><header>Use of fees and limitation</header><text>The fees authorized by this section shall be collected and available only to defray the costs of cosmetic safety activities.</text>
</subparagraph><subparagraph commented="no" id="H39881D8D5AF146609ACFC3FA29993609"><enum>(C)</enum><header>Fee collections during first program year</header><text display-inline="yes-display-inline">Until the date of enactment of discretionary appropriations through September 30, 2020, for the <quote>Food and Drug Administration—Salaries and Expenses</quote> account, fees authorized by this section for fiscal year 2020 may be collected, and any fees so collected shall be credited to such account, to remain available until expended.</text>
</subparagraph><subparagraph commented="no" id="H47D1534A2A8C4FCF9F015580744B5353"><enum>(D)</enum><header>Startup costs</header><text display-inline="yes-display-inline">Until one year after the Secretary begins collecting user fees under subsection (a), any amounts available for the Center for Food Safety and Applied Nutrition and related field activities (excluding user fees) shall be available and allocated as needed to pay the costs of any cosmetic safety activities not authorized before enactment of the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title>.</text>
</subparagraph><subparagraph commented="no" id="H6D1266CF3A09442FAFA0B64849D21453"><enum>(E)</enum><header>Reimbursement of startup amounts</header>
<clause commented="no" id="H082B8C43EF634C96A70A527E01E11632"><enum>(i)</enum><header>In general</header><text display-inline="yes-display-inline">Any amounts allocated for the startup period pursuant to subparagraph (D) shall be reimbursed through any appropriated fees collected under subsection (a), in such manner as the Secretary determines appropriate to ensure that such allocation results in no net change in the total amount of funds otherwise available, for a period not to exceed two years after the Secretary begins collecting user fees under subsection (a), for the Center for Food Safety and Applied Nutrition and related field activities (other than cosmetic safety activities and related field activities funded through such allocation) for such period.</text>
</clause><clause commented="no" id="HB6BAFE70D79B47C3AE3C3788B3856DC4"><enum>(ii)</enum><header>Treatment of reimbursed amounts</header><text>Amounts reimbursed under clause (i) shall be available for the programs and activities for which funds allocated for the startup period were available, prior to such allocation, until 1 year after the Secretary begins collecting user fees under subsection (a), notwithstanding any otherwise applicable limits on amounts for such programs or activities for a fiscal year.</text>
</clause></subparagraph></paragraph><paragraph commented="no" id="HBC2B0D18F8B24139949DC86F62AC7644"><enum>(3)</enum><header>Authorization of appropriations</header><text>There are authorized to be appropriated for fees under this section the following:</text> <subparagraph commented="no" id="HD2834CC5A18E490ABD9EB49A7608AC62"><enum>(A)</enum><text>$10,000,000 for fiscal year 2020;</text>
</subparagraph><subparagraph commented="no" id="HA5971282F556494DB3871BFFCA73BCCB"><enum>(B)</enum><text>$20,000,000 for fiscal year 2021;</text> </subparagraph><subparagraph commented="no" id="HDA1751D9ACF14AE7BC3CFC96BDD38B0C"><enum>(C)</enum><text>$35,000,000 for fiscal year 2022; and</text>
</subparagraph><subparagraph commented="no" id="HC6B0D4736C3E47B5BC83844DFAA1438C"><enum>(D)</enum><text>$46,000,000 for each of fiscal years 2023 through 2027.</text> </subparagraph></paragraph></subsection><subsection commented="no" id="HE3A2E0E8EE4A4E7EB338B73BFA8BA6C0"><enum>(g)</enum><header>Effect of failure To pay fees</header><text display-inline="yes-display-inline">The Secretary shall not consider a registration by a responsible person submitted under section 605 to be complete until all fees owed by such person under subsection (a) are paid. Until the fees are paid, the registration is incomplete and the responsible person is deemed to have failed to register in accordance with section 605.</text>
</subsection><subsection commented="no" id="H8733847652F349BFBA16838A842CAA7A"><enum>(h)</enum><header>Collection of unpaid fees</header><text>In any case where the Secretary does not receive payment of a fee assessed under subsection (a), such fee shall be treated as a claim of the United States Government subject to subchapter II of <external-xref legal-doc="usc-chapter" parsable-cite="usc-chapter/31/37">chapter 37</external-xref> of title 31, United States Code.</text>
</subsection><subsection commented="no" id="H16EF38D5D3E440D4B3066EA5A1378254"><enum>(i)</enum><header>Construction</header><text>This section may not be construed to require that the number of full-time equivalent positions in the Department of Health and Human Services, for officers, employees, and advisory committees not engaged in cosmetic safety activities, be reduced to offset the number of officers, employees, and advisory committees so engaged.</text>
</subsection><subsection commented="no" id="H5A21A76E464B428884ED212205EF8B9C"><enum>(j)</enum><header>Records</header><text display-inline="yes-display-inline">Each responsible person that is required to register under section 605 shall retain all records necessary to demonstrate gross annual sales for at least 2 fiscal years after such information is reported in its registration. Such records shall be made available to the Secretary for review and duplication upon request of the Secretary.</text>
</subsection><subsection commented="no" id="HA713F7D195AC45A5A4B5EB1A0A3DA061"><enum>(k)</enum><header>Limitation</header><text>This part does not authorize the assessment or collection of a fee for registration under section 605 occurring after fiscal year 2027.</text></subsection></section></part><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section commented="no" id="HE3C5FE002D024D149454F5539C90851B"><enum>203.</enum><header>Direct hiring authority to support activities related to cosmetics</header><text display-inline="no-display-inline">Part 10 of subchapter C of chapter VII, as added by section 202, is amended by inserting after section 744M the following:</text>
<quoted-block display-inline="no-display-inline" id="H7214B93589F541749B1EF7F9AA68E41C" style="OLC">
<section commented="no" id="HE08350F6C4834848B45587C71F854D5B"><enum>744N.</enum><header>Direct hiring authority to support activities related to cosmetics</header>
<text display-inline="no-display-inline">The Secretary shall have direct hiring authority with respect to the appointment of employees into the competitive service or the excepted service to administer the <short-title>Cosmetic Safety Enhancement Act of 2019</short-title> and the amendments made thereby.</text>
</section><section commented="no" id="H02311D67093243F09B050045CC6C7FA8"><enum>744O.</enum><header>Reporting requirements; reauthorization</header>
<subsection commented="no" id="HE216086AAEE7420BADD8958074A6EE26"><enum>(a)</enum><header>Performance report</header><text>Beginning with fiscal year 2021, and not later than 120 calendar days after the end of each fiscal year thereafter for which fees are collected under this part, the Secretary shall prepare and submit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Health, Education, Labor, and Pensions of the Senate a report concerning the progress of the Food and Drug Administration on cosmetic safety activities during such fiscal year, including the future plans of the Food and Drug Administration for such activities.</text>
</subsection><subsection commented="no" id="H9FE52625D81E4EF29F3C37E47698C234"><enum>(b)</enum><header>Fiscal report</header><text>Not later than 120 calendar days after the end of fiscal year 2021 and each subsequent fiscal year for which fees are collected under this part, the Secretary shall prepare and submit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Health, Education, Labor, and Pensions of the Senate a report on the implementation of the authority for such fees during such fiscal year and the use, by the Food and Drug Administration, of the fees collected for such fiscal year.</text>
</subsection><subsection commented="no" id="HBF41D4AA5F6441DA99AC16B41F19DF35"><enum>(c)</enum><header>Public availability</header><text>The Secretary shall make the reports required under subsections (a) and (b) available to the public on the internet website of the Food and Drug Administration.</text>
</subsection><subsection commented="no" id="H9278DA6627FF45B4A077D36827B7B524"><enum>(d)</enum><header>Reauthorization</header>
<paragraph commented="no" id="HC2418FC2016E40049A9B1D89452395A3"><enum>(1)</enum><header>Consultation</header><text>In developing recommendations to present to the Congress with respect to performance goals developed by the Food and Drug Administration, and plans for meeting the goals, for cosmetic safety activities for the first 5 fiscal years after fiscal year 2027, and for the reauthorization of this part for such fiscal years, the Secretary shall consult with—</text>
<subparagraph commented="no" id="H204AB8B713E4441D90ACF72177724070"><enum>(A)</enum><text>the Committee on Energy and Commerce of the House of Representatives;</text> </subparagraph><subparagraph commented="no" id="H3D485426F1614F15A782360E8C04C421"><enum>(B)</enum><text>the Committee on Health, Education, Labor, and Pensions of the Senate;</text>
</subparagraph><subparagraph commented="no" id="HFD9E3F6A6D434A17B36D77AC2C8CD922"><enum>(C)</enum><text>scientific and academic experts;</text> </subparagraph><subparagraph commented="no" id="H5FD7640C98AA4D438743C2809A475585"><enum>(D)</enum><text>health care professionals;</text>
</subparagraph><subparagraph commented="no" id="HC0EAF5E79AF44D32AF5F06CA580339A9"><enum>(E)</enum><text>representatives of public health and consumer advocacy groups; and</text> </subparagraph><subparagraph commented="no" id="H680C17DD2D774535AAAB0E59759CD85C"><enum>(F)</enum><text>the regulated industry.</text>
</subparagraph></paragraph><paragraph commented="no" id="HC5997536D0B24F2182845379ABF95A3E"><enum>(2)</enum><header>Public review of recommendations</header><text>After negotiations with the regulated industry, the Secretary shall—</text> <subparagraph commented="no" id="H010A0C1C07EE400C96026F6FBFB1C077"><enum>(A)</enum><text>present the recommendations developed under paragraph (1) to the congressional committees specified in such paragraph;</text>
</subparagraph><subparagraph commented="no" id="H7F5FAC067FA1406580A7CC14718600FF"><enum>(B)</enum><text>publish such recommendations in the Federal Register;</text> </subparagraph><subparagraph commented="no" id="H115BF22FF56F4905B29223554CC27A3F"><enum>(C)</enum><text>provide for a period of 30 calendar days for the public to provide written comments on such recommendations;</text>
</subparagraph><subparagraph commented="no" id="HED184002BE9F47E39CE3CCC32D7089A3"><enum>(D)</enum><text>hold a meeting at which the public may present its views on such recommendations; and</text> </subparagraph><subparagraph commented="no" id="H6B982AB8F15E4CF1B5D51D22785BC1BD"><enum>(E)</enum><text>after consideration of such public views and comments, revise such recommendations as necessary.</text>
</subparagraph></paragraph><paragraph commented="no" id="H43112DF730B64BCF96E4DAA9C8850B02"><enum>(3)</enum><header>Transmittal of recommendations</header><text>Not later than January 15, 2026, the Secretary shall transmit to the Congress the revised recommendations under paragraph (2), a summary of the views and comments received under such paragraph, and any changes made to the recommendations in response to such views and comments.</text></paragraph></subsection></section><after-quoted-block>.</after-quoted-block></quoted-block>
</section><section id="HA0C7A1BA3E5F40A08C2F3E64A293D9C9"><enum>204.</enum><header>Sunset dates</header>
<subsection id="H455DFC29E674401FB639C472D0A590FE"><enum>(a)</enum><header>Authorization</header><text display-inline="yes-display-inline">Sections 744L, 744M, and 744N of the Federal Food, Drug, and Cosmetic Act, as added by section 202, shall cease to be effective October 1, 2027.</text>
</subsection><subsection id="HB08259C069CB49E1B40A8D2976BA2281"><enum>(b)</enum><header>Reporting requirements</header><text>Section 744O of the Federal Food, Drug, and Cosmetic Act, as added by section 203, shall cease to be effective January 31, 2028.</text>
</subsection></section>